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Pathways
Variants search result for Homo sapiens
(View Results for all Objects and Ontologies)


1001 records found for search term Glb1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
11589763CV290780single nucleotide variantNM_000404.4(GLB1):c.-25C>GGM1 gangliosidosis [RCV000270068]|Mucopolysaccharidosis, MPS-IV-B [RCV000313297]|not provided [RCV004694734]uncertain significance33309711033097110Human2name
11595773CV293948single nucleotide variantNM_000404.4(GLB1):c.-37C>GGM1 gangliosidosis [RCV000330888]|Mucopolysaccharidosis, MPS-IV-B [RCV000374183]|not specified [RCV000593706]benign|uncertain significance33309712233097122Human2name
11582947CV293951single nucleotide variantNM_000404.3(GLB1):c.-73C>TGM1 gangliosidosis [RCV000315931]|Morquio syndrome [RCV000263130]uncertain significance33309715833097158Human2name
11646887CV294412single nucleotide variantNM_000404.4(GLB1):c.-35T>GGM1 gangliosidosis [RCV000273433]|Morquio syndrome [RCV000370265]uncertain significance33309712033097120Human2name
28877740CV888666single nucleotide variantNM_000404.4(GLB1):c.*44C>TGM1 gangliosidosis [RCV001148444]|Mucopolysaccharidosis, MPS-IV-B [RCV001148443]uncertain significance33299700132997001Human2name
28882664CV888667single nucleotide variantNM_000404.4(GLB1):c.*39C>TGM1 gangliosidosis [RCV001150008]|Mucopolysaccharidosis, MPS-IV-B [RCV001150007]uncertain significance33299700632997006Human2name
28872326CV888674single nucleotide variantNM_000404.4(GLB1):c.-17C>TGM1 gangliosidosis [RCV001146236]|Mucopolysaccharidosis, MPS-IV-B [RCV001146235]uncertain significance33309710233097102Human2name
28879546CV888675single nucleotide variantNM_000404.4(GLB1):c.-48G>CGM1 gangliosidosis [RCV001149030]|Mucopolysaccharidosis, MPS-IV-B [RCV001149031]likely benign|uncertain significance33309713333097133Human2name
127233854CV1065829single nucleotide variantNM_000404.4(GLB1):c.75+2T>GMucopolysaccharidosis, MPS-IV-B [RCV001391310]pathogenic33309700933097009Human1name
127282508CV1070703single nucleotide variantNM_000404.4(GLB1):c.76-4G>AMucopolysaccharidosis, MPS-IV-B [RCV001411159]likely benign33307271733072717Human1name
127260083CV1092388single nucleotide variantNM_000404.4(GLB1):c.76-9G>AMucopolysaccharidosis, MPS-IV-B [RCV001427721]likely benign33307272233072722Human1name
151351399CV1323587duplicationNM_000404.4(GLB1):c.75+4dupInfantile GM1 gangliosidosis [RCV001806443]pathogenic33309700633097007Human1name , alternate_id
8555885CV15975duplicationNM_000404.4(GLB1):c.75+2dupGM1 gangliosidosis type 2 [RCV003338377]|GM1 gangliosidosis type 3 [RCV001376158]|Inborn genetic diseases [RCV004975256]|Infantile GM1 gangliosidosis [RCV000000985]|Mucopolysaccharidosis, MPS-IV-B [RCV000781443]|Mucopolysaccharidosis, MPS-IV-B [RCV000796145]|not provided [RCV000412989]pathogenic33309700833097009Human5name , alternate_id
152026572CV1626515single nucleotide variantNM_000404.4(GLB1):c.75+7C>GMucopolysaccharidosis, MPS-IV-B [RCV002185200]likely benign33309700433097004Human1name
152135464CV1634450single nucleotide variantNM_000404.4(GLB1):c.75+9G>AMucopolysaccharidosis, MPS-IV-B [RCV002218654]likely benign33309700233097002Human1name
156205056CV1905845single nucleotide variantNM_000404.4(GLB1):c.76-5T>CMucopolysaccharidosis, MPS-IV-B [RCV003084367]likely benign33307271833072718Human1name
155958048CV2087126deletionNM_000404.4(GLB1):c.75+8delMucopolysaccharidosis, MPS-IV-B [RCV002862716]likely benign33309700333097003Human1name
156377726CV2120787single nucleotide variantNM_000404.4(GLB1):c.76-9G>TMucopolysaccharidosis, MPS-IV-B [RCV002942881]likely benign33307272233072722Human1name
11350571CV237277single nucleotide variantNM_000404.4(GLB1):c.75+3A>GMucopolysaccharidosis, MPS-IV-B [RCV002516236]|not provided [RCV000223994]|not specified [RCV003155132]uncertain significance33309700833097008Human1name
11595177CV290008single nucleotide variantNM_000404.4(GLB1):c.*354T>CGM1 gangliosidosis [RCV000331429]|Mucopolysaccharidosis, MPS-IV-B [RCV000367464]|not provided [RCV004709953]benign|likely benign33299669132996691Human2name
11582999CV290009single nucleotide variantNM_000404.4(GLB1):c.*319G>AGM1 gangliosidosis [RCV000318566]|Mucopolysaccharidosis, MPS-IV-B [RCV000263456]|not provided [RCV003430878]benign|conflicting interpretations of pathogenicity|uncertain significance33299672632996726Human2name
11593293CV290015single nucleotide variantNM_000404.4(GLB1):c.*182A>GGM1 gangliosidosis [RCV000282978]|Mucopolysaccharidosis, MPS-IV-B [RCV000347304]benign|uncertain significance33299686332996863Human2name
11584822CV290770single nucleotide variantNM_000404.4(GLB1):c.*376C>GGM1 gangliosidosis [RCV000371297]|Mucopolysaccharidosis, MPS-IV-B [RCV000276748]likely benign|uncertain significance33299666932996669Human2name
11647895CV290771single nucleotide variantNM_000404.4(GLB1):c.*194C>AGM1 gangliosidosis [RCV000373349]|Mucopolysaccharidosis, MPS-IV-B [RCV000278820]uncertain significance33299685132996851Human2name
11590981CV290772single nucleotide variantNM_000404.4(GLB1):c.*184G>AGM1 gangliosidosis [RCV000379183]|Mucopolysaccharidosis, MPS-IV-B [RCV000324599]likely benign|uncertain significance33299686132996861Human2name
11589001CV293940single nucleotide variantNM_000404.4(GLB1):c.*423A>GGM1 gangliosidosis [RCV000270965]|Mucopolysaccharidosis, MPS-IV-B [RCV000307361]uncertain significance33299662232996622Human2name
405061719CV3108522single nucleotide variantNM_000404.4(GLB1):c.76-1G>TMucopolysaccharidosis, MPS-IV-B [RCV003809100]likely pathogenic33307271433072714Human1name
28871108CV888665single nucleotide variantNM_000404.4(GLB1):c.*224G>TGM1 gangliosidosis [RCV001145681]|Mucopolysaccharidosis, MPS-IV-B [RCV001145682]uncertain significance33299682132996821Human2name
8639837CV98820single nucleotide variantNM_000404.4(GLB1):c.75+1G>Cnot provided [RCV000173120]pathogenic|uncertain significance33309701033097010Humanname
126731019CV1000392single nucleotide variantNM_000404.4(GLB1):c.457+3A>Cnot provided [RCV001310483]uncertain significance33306822733068227Humanname
127249497CV1070692single nucleotide variantNM_000404.4(GLB1):c.914+7G>CMucopolysaccharidosis, MPS-IV-B [RCV001417333]likely benign33305187633051876Human1name
127255244CV1092380single nucleotide variantNM_000404.4(GLB1):c.955+8C>TMucopolysaccharidosis, MPS-IV-B [RCV001426506]likely benign33305175033051750Human1name
127255075CV1092389single nucleotide variantNM_000404.4(GLB1):c.75+10C>TMucopolysaccharidosis, MPS-IV-B [RCV001437395]likely benign33309700133097001Human1name
127312001CV1134792single nucleotide variantNM_000404.4(GLB1):c.956-6T>CMucopolysaccharidosis, MPS-IV-B [RCV001501781]likely benign33304623833046238Human1name
127337867CV1134797single nucleotide variantNM_000404.4(GLB1):c.792+9C>AMucopolysaccharidosis, MPS-IV-B [RCV001493218]likely benign33305348233053482Human1name
150422232CV1179693single nucleotide variantNM_000404.4(GLB1):c.75+90G>Tnot provided [RCV001552438]likely benign33309692133096921Humanname
151716654CV1342977single nucleotide variantNM_000404.4(GLB1):c.734-6T>AMucopolysaccharidosis, MPS-IV-B [RCV002024123]likely benign|uncertain significance33305355533053555Human1name
151831814CV1364693single nucleotide variantNM_000404.4(GLB1):c.915-1G>TMucopolysaccharidosis, MPS-IV-B [RCV001985845]likely pathogenic33305179933051799Human1name
151794516CV1409814single nucleotide variantNM_000404.4(GLB1):c.246-2A>GMucopolysaccharidosis, MPS-IV-B [RCV001910472]pathogenic33306897233068972Human1name
152025856CV1528113single nucleotide variantNM_000404.4(GLB1):c.552+8T>CMucopolysaccharidosis, MPS-IV-B [RCV002084605]likely benign33306545533065455Human1name
152091589CV1528788single nucleotide variantNM_000404.4(GLB1):c.733+7G>AMucopolysaccharidosis, MPS-IV-B [RCV002094257]likely benign33305808233058082Human1name
152145096CV1543227single nucleotide variantNM_000404.4(GLB1):c.915-8C>GMucopolysaccharidosis, MPS-IV-B [RCV002178601]likely benign33305180633051806Human1name
152111871CV1558833single nucleotide variantNM_000404.4(GLB1):c.915-4G>AMucopolysaccharidosis, MPS-IV-B [RCV002134587]likely benign33305180233051802Human1name
152085629CV1621051single nucleotide variantNM_000404.4(GLB1):c.793-9T>AMucopolysaccharidosis, MPS-IV-B [RCV002193594]likely benign33305201333052013Human1name
152982414CV1677351single nucleotide variantNM_000404.4(GLB1):c.553-2A>TGLB1-related disorder [RCV004698866]|Infantile GM1 gangliosidosis [RCV002249057]|Mucopolysaccharidosis, MPS-IV-B [RCV003094010]pathogenic|likely pathogenic33305827133058271Human3name , alternate_id
156274263CV1900121single nucleotide variantNM_000404.4(GLB1):c.792+9C>TMucopolysaccharidosis, MPS-IV-B [RCV003086894]likely benign33305348233053482Human1name
156406970CV1917939single nucleotide variantNM_000404.4(GLB1):c.955+5G>AMucopolysaccharidosis, MPS-IV-B [RCV002606758]pathogenic|uncertain significance33305175333051753Human1name
156386223CV1999234single nucleotide variantNM_000404.4(GLB1):c.458-5T>CMucopolysaccharidosis, MPS-IV-B [RCV002654008]likely benign33306556233065562Human1name
156138578CV2032824single nucleotide variantNM_000404.4(GLB1):c.397-8T>CMucopolysaccharidosis, MPS-IV-B [RCV002740816]likely benign33306829833068298Human1name
156166032CV2075275single nucleotide variantNM_000404.4(GLB1):c.396+7G>TMucopolysaccharidosis, MPS-IV-B [RCV002851386]likely benign33306881333068813Human1name
156113097CV2136280single nucleotide variantNM_000404.4(GLB1):c.457+3A>GMucopolysaccharidosis, MPS-IV-B [RCV003002676]uncertain significance33306822733068227Human1name
156071290CV2163511single nucleotide variantNM_000404.4(GLB1):c.76-17C>TMucopolysaccharidosis, MPS-IV-B [RCV003020048]likely benign33307273033072730Human1name
156116230CV2182943single nucleotide variantNM_000404.4(GLB1):c.245+3A>GMucopolysaccharidosis, MPS-IV-B [RCV003039136]uncertain significance33307254133072541Human1name
156027185CV2185672single nucleotide variantNM_000404.4(GLB1):c.245+6T>CMucopolysaccharidosis, MPS-IV-B [RCV003036020]uncertain significance33307253833072538Human1name
329848877CV2523627single nucleotide variantNM_000404.4(GLB1):c.733+6T>CGM1 gangliosidosis [RCV003225641]pathogenic33305808333058083Human1name
11655619CV290019single nucleotide variantNM_000404.4(GLB1):c.553-8A>GGM1 gangliosidosis [RCV000388761]|Mucopolysaccharidosis, MPS-IV-B [RCV000326950]uncertain significance33305827733058277Human2name
402521130CV3091988single nucleotide variantNM_000404.4(GLB1):c.552+7C>GMucopolysaccharidosis, MPS-IV-B [RCV003790434]likely benign33306545633065456Human1name
405048762CV3097504single nucleotide variantNM_000404.4(GLB1):c.552+1G>AMucopolysaccharidosis, MPS-IV-B [RCV003808084]pathogenic33306546233065462Human1name
405033976CV3098778single nucleotide variantNM_000404.4(GLB1):c.75+20G>AMucopolysaccharidosis, MPS-IV-B [RCV003806904]likely benign33309699133096991Human1name
404980745CV3099642single nucleotide variantNM_000404.4(GLB1):c.914+5G>AMucopolysaccharidosis, MPS-IV-B [RCV003791471]uncertain significance33305187833051878Human1name
405077797CV3100418single nucleotide variantNM_000404.4(GLB1):c.75+19G>AMucopolysaccharidosis, MPS-IV-B [RCV003799971]likely benign33309699233096992Human1name
405180984CV3101794single nucleotide variantNM_000404.4(GLB1):c.396+9G>AMucopolysaccharidosis, MPS-IV-B [RCV003804008]likely benign33306881133068811Human1name
405015472CV3104455single nucleotide variantNM_000404.4(GLB1):c.915-2A>GMucopolysaccharidosis, MPS-IV-B [RCV003805324]likely pathogenic33305180033051800Human1name
405151255CV3105729single nucleotide variantNM_000404.4(GLB1):c.956-4C>AMucopolysaccharidosis, MPS-IV-B [RCV003801446]likely benign33304623633046236Human1name
405037523CV3106303single nucleotide variantNM_000404.4(GLB1):c.76-12C>AMucopolysaccharidosis, MPS-IV-B [RCV003796994]likely benign33307272533072725Human1name
405059722CV3108338single nucleotide variantNM_000404.4(GLB1):c.75+16C>TMucopolysaccharidosis, MPS-IV-B [RCV003808916]likely benign33309699533096995Human1name
405065716CV3108967deletionNM_000404.4(GLB1):c.76-16delMucopolysaccharidosis, MPS-IV-B [RCV003809377]benign33307272933072729Human1name
596944554CV3543242single nucleotide variantNM_000404.4(GLB1):c.914+4A>GGM1 gangliosidosis [RCV004799114]likely pathogenic33305187933051879Human1name
12742726CV359420single nucleotide variantNM_000404.4(GLB1):c.396+2T>CMucopolysaccharidosis, MPS-IV-B [RCV003766144]|not provided [RCV000414347]pathogenic|likely pathogenic33306881833068818Human1name
597880032CV3872128single nucleotide variantNM_000404.4(GLB1):c.75+16C>AMucopolysaccharidosis, MPS-IV-B [RCV005217180]likely benign33309699533096995Human1name
598126537CV3881986single nucleotide variantNM_000404.4(GLB1):c.955+2T>AGLB1-related disorder [RCV005233538]pathogenic33305175633051756Humanname , trait
12898467CV404764single nucleotide variantNM_000404.4(GLB1):c.245+1G>AGM1 gangliosidosis [RCV001175540]|GM1 gangliosidosis type 2 [RCV000477865]|Mucopolysaccharidosis, MPS-IV-B [RCV000685614]|not provided [RCV004591410]pathogenic|likely pathogenic33307254333072543Human3name , alternate_id
13792276CV542941single nucleotide variantNM_000404.4(GLB1):c.733+1G>AGM1 gangliosidosis type 2 [RCV000668507]|Mucopolysaccharidosis, MPS-IV-B [RCV001203710]|not provided [RCV001784254]pathogenic|likely pathogenic33305808833058088Human2name , alternate_id
13782683CV542948single nucleotide variantNM_000404.4(GLB1):c.552+2T>CGM1 gangliosidosis type 2 [RCV000669176]|Mucopolysaccharidosis, MPS-IV-B [RCV002532083]likely pathogenic33306546133065461Human2name , alternate_id
13783899CV543122single nucleotide variantNM_000404.4(GLB1):c.245+1G>CGM1 gangliosidosis type 2 [RCV000670410]|Mucopolysaccharidosis, MPS-IV-B [RCV002531251]pathogenic|likely pathogenic33307254333072543Human2name , alternate_id
14703041CV651170single nucleotide variantNM_000404.4(GLB1):c.553-1G>CMucopolysaccharidosis, MPS-IV-B [RCV000791815]pathogenic33305827033058270Human1name
15132203CV695198single nucleotide variantNM_000404.4(GLB1):c.397-5A>GMucopolysaccharidosis, MPS-IV-B [RCV000876110]likely benign33306829533068295Human1name
38456577CV940748single nucleotide variantNM_000404.4(GLB1):c.734-2A>GMucopolysaccharidosis, MPS-IV-B [RCV001217818]pathogenic33305355133053551Human1name
38459469CV959694single nucleotide variantNM_000404.4(GLB1):c.955+2T>GGM1 gangliosidosis type 2 [RCV005036493]|Mucopolysaccharidosis, MPS-IV-B [RCV001225769]likely pathogenic33305175633051756Human2name , alternate_id
40903268CV975775single nucleotide variantNM_000404.4(GLB1):c.733+2T>CMucopolysaccharidosis, MPS-IV-B [RCV001269210]|Mucopolysaccharidosis, MPS-IV-B [RCV003770401]pathogenic|likely pathogenic33305808733058087Human1name
8639830CV98813single nucleotide variantNM_000404.4(GLB1):c.397-1G>AGM1 gangliosidosis type 2 [RCV000667741]|Mucopolysaccharidosis, MPS-IV-B [RCV001211514]|not provided [RCV000178086]pathogenic|likely pathogenic33306829133068291Human2name , alternate_id
8639832CV98815single nucleotide variantNM_000404.4(GLB1):c.457+2T>CMucopolysaccharidosis, MPS-IV-B [RCV003764757]|not provided [RCV000178088]pathogenic|likely pathogenic33306822833068228Human1name
8639836CV98819single nucleotide variantNM_000404.4(GLB1):c.734-8A>GGM1 gangliosidosis [RCV002508193]|GM1 gangliosidosis type 2 [RCV000669168]|not provided [RCV000078720]|not specified [RCV003317082]uncertain significance|not provided33305355733053557Human2name , alternate_id
127255184CV1070685single nucleotide variantNM_000404.4(GLB1):c.1735-8C>TMucopolysaccharidosis, MPS-IV-B [RCV001418693]likely benign33299735232997352Human1name
127263587CV1070689deletionNM_000404.4(GLB1):c.1480-8delMucopolysaccharidosis, MPS-IV-B [RCV001403043]likely benign33301431833014318Human1name
127271189CV1092385single nucleotide variantNM_000404.4(GLB1):c.734-10C>AMucopolysaccharidosis, MPS-IV-B [RCV001441734]likely benign33305355933053559Human1name
127335913CV1113899single nucleotide variantNM_000404.4(GLB1):c.1480-4G>TMucopolysaccharidosis, MPS-IV-B [RCV001474604]likely benign33301431433014314Human1name
127334033CV1113900single nucleotide variantNM_000404.4(GLB1):c.1480-5T>CMucopolysaccharidosis, MPS-IV-B [RCV001473330]likely benign33301431533014315Human1name
127297304CV1113902single nucleotide variantNM_000404.4(GLB1):c.1347+9C>TMucopolysaccharidosis, MPS-IV-B [RCV001477576]likely benign33301843933018439Human1name
127295657CV1113909single nucleotide variantNM_000404.4(GLB1):c.915-10T>CMucopolysaccharidosis, MPS-IV-B [RCV001459789]likely benign33305180833051808Human1name
127318538CV1134795single nucleotide variantNM_000404.4(GLB1):c.792+10G>CMucopolysaccharidosis, MPS-IV-B [RCV001483553]likely benign33305348133053481Human1name
127335985CV1134796single nucleotide variantNM_000404.4(GLB1):c.792+10G>AGLB1-related disorder [RCV004738322]|Mucopolysaccharidosis, MPS-IV-B [RCV001491856]likely benign33305348133053481Human2name
127301242CV1154461duplicationNM_000404.4(GLB1):c.793-14dupMucopolysaccharidosis, MPS-IV-B [RCV001514568]benign33305201133052012Human1name
127299871CV1154462single nucleotide variantNM_000404.4(GLB1):c.792+18G>AMucopolysaccharidosis, MPS-IV-B [RCV001513874]benign33305347333053473Human1name
127287679CV1163124single nucleotide variantNM_000404.4(GLB1):c.734-80G>AInfantile GM1 gangliosidosis [RCV001527561]|Mucopolysaccharidosis, MPS-IV-B [RCV001527562]|not provided [RCV001538541]benign|likely benign33305362933053629Human2name , alternate_id
127287682CV1163125single nucleotide variantNM_000404.4(GLB1):c.734-99G>TInfantile GM1 gangliosidosis [RCV001527563]|Mucopolysaccharidosis, MPS-IV-B [RCV001527564]|not provided [RCV001692445]benign33305364833053648Human2name , alternate_id
127287689CV1163127single nucleotide variantNM_000404.4(GLB1):c.733+78A>GInfantile GM1 gangliosidosis [RCV001527567]|Mucopolysaccharidosis, MPS-IV-B [RCV001527568]|not provided [RCV001615231]benign|likely benign33305801133058011Human2name , alternate_id
150423733CV1183323single nucleotide variantNM_000404.4(GLB1):c.245+44A>Cnot provided [RCV001555723]likely benign33307250033072500Humanname
150407388CV1190038single nucleotide variantNM_000404.4(GLB1):c.76-288A>Gnot provided [RCV001565000]likely benign33307300133073001Humanname
150404322CV1193294single nucleotide variantNM_000404.4(GLB1):c.457+53C>Anot provided [RCV001571053]likely benign33306817733068177Humanname
150474556CV1202117single nucleotide variantNM_000404.4(GLB1):c.396+61G>Anot provided [RCV001589360]likely benign33306875933068759Humanname
150434789CV1206835single nucleotide variantNM_000404.4(GLB1):c.793-69T>Cnot provided [RCV001582184]likely benign33305207333052073Humanname
150485306CV1273851deletionNM_000404.4(GLB1):c.955+93delnot provided [RCV001698695]benign33305166533051665Humanname
151791685CV1409049single nucleotide variantNM_000404.4(GLB1):c.1479+1G>CMucopolysaccharidosis, MPS-IV-B [RCV001905463]pathogenic33301670833016708Human1name
151716769CV1433757single nucleotide variantNM_000404.4(GLB1):c.1234-8C>GMucopolysaccharidosis, MPS-IV-B [RCV002024478]likely benign|uncertain significance33301856933018569Human1name
151815833CV1467635single nucleotide variantNM_000404.4(GLB1):c.1143+3A>CMucopolysaccharidosis, MPS-IV-B [RCV001952589]uncertain significance33302424833024248Human1name
151790945CV1480519single nucleotide variantNM_000404.4(GLB1):c.552+18C>TMucopolysaccharidosis, MPS-IV-B [RCV001903911]likely benign|uncertain significance33306544533065445Human1name
152082579CV1525180single nucleotide variantNM_000404.4(GLB1):c.1069-8G>TMucopolysaccharidosis, MPS-IV-B [RCV002131009]|not provided [RCV004711865]likely benign33302433333024333Human1name
152155753CV1561012single nucleotide variantNM_000404.4(GLB1):c.1068+7G>AMucopolysaccharidosis, MPS-IV-B [RCV002102904]likely benign33304611333046113Human1name
152174923CV1572790single nucleotide variantNM_000404.4(GLB1):c.792+19G>AMucopolysaccharidosis, MPS-IV-B [RCV002144603]likely benign33305347233053472Human1name
152026944CV1583212single nucleotide variantNM_000404.4(GLB1):c.793-20A>GMucopolysaccharidosis, MPS-IV-B [RCV002084967]likely benign33305202433052024Human1name
8555886CV15985single nucleotide variantNM_000404.4(GLB1):c.1480-2A>GGM1 gangliosidosis [RCV001251276]|GM1 gangliosidosis type 2 [RCV002496221]|GM1-gangliosidosis, type I, with cardiac involvement [RCV000000996]|Infantile GM1 gangliosidosis [RCV002470702]|Mucopolysaccharidosis, MPS-IV-B [RCV000790562]|Mucopolysaccharidosis, MPS-IV-B [RCV001049270]|not provided [RCV00pathogenic33301431233014312Human4name , alternate_id
152172270CV1599055single nucleotide variantNM_000404.4(GLB1):c.915-17C>AMucopolysaccharidosis, MPS-IV-B [RCV002143721]likely benign33305181533051815Human1name
152069014CV1640099single nucleotide variantNM_000404.4(GLB1):c.1735-4C>GMucopolysaccharidosis, MPS-IV-B [RCV002147822]likely benign33299734832997348Human1name
152064950CV1652473single nucleotide variantNM_000404.4(GLB1):c.1480-9G>AMucopolysaccharidosis, MPS-IV-B [RCV002090768]likely benign33301431933014319Human1name
152173550CV1662692single nucleotide variantNM_000404.4(GLB1):c.553-17T>CMucopolysaccharidosis, MPS-IV-B [RCV002144143]likely benign33305828633058286Human1name
156363487CV1881522single nucleotide variantNM_000404.4(GLB1):c.397-11C>TMucopolysaccharidosis, MPS-IV-B [RCV003065790]likely benign33306830133068301Human1name
156418502CV1922247single nucleotide variantNM_000404.4(GLB1):c.457+19C>TMucopolysaccharidosis, MPS-IV-B [RCV002611699]likely benign33306821133068211Human1name
156283176CV1929584single nucleotide variantNM_000404.4(GLB1):c.246-11T>GMucopolysaccharidosis, MPS-IV-B [RCV002628504]likely benign33306898133068981Human1name
155963576CV1931768single nucleotide variantNM_000404.4(GLB1):c.1234-3C>AMucopolysaccharidosis, MPS-IV-B [RCV002616849]uncertain significance33301856433018564Human1name
156230312CV1959132single nucleotide variantNM_000404.4(GLB1):c.1734+4C>TMucopolysaccharidosis, MPS-IV-B [RCV002596784]uncertain significance33301405233014052Human1name
156050990CV1974367single nucleotide variantNM_000404.4(GLB1):c.793-18G>AMucopolysaccharidosis, MPS-IV-B [RCV002590660]likely benign33305202233052022Human1name
155971793CV1978452single nucleotide variantNM_000404.4(GLB1):c.914+15C>TMucopolysaccharidosis, MPS-IV-B [RCV002617216]likely benign33305186833051868Human1name
156080176CV1982691single nucleotide variantNM_000404.4(GLB1):c.396+11C>GMucopolysaccharidosis, MPS-IV-B [RCV002638873]likely benign33306880933068809Human1name
156344923CV1995106single nucleotide variantNM_000404.4(GLB1):c.1347+1G>TGM1 gangliosidosis type 2 [RCV005034358]|Mucopolysaccharidosis, MPS-IV-B [RCV002650519]likely pathogenic33301844733018447Human2name , alternate_id
156176015CV2000406single nucleotide variantNM_000404.4(GLB1):c.246-10G>TMucopolysaccharidosis, MPS-IV-B [RCV002642873]likely benign33306898033068980Human1name
156369095CV2007568single nucleotide variantNM_000404.4(GLB1):c.1735-8C>GMucopolysaccharidosis, MPS-IV-B [RCV002676770]likely benign33299735232997352Human1name
156332475CV2075953single nucleotide variantNM_000404.4(GLB1):c.733+13A>TMucopolysaccharidosis, MPS-IV-B [RCV002835376]likely benign33305807633058076Human1name
156010411CV2079597single nucleotide variantNM_000404.4(GLB1):c.397-19C>TMucopolysaccharidosis, MPS-IV-B [RCV002866074]likely benign33306830933068309Human1name
155916774CV2091805single nucleotide variantNM_000404.4(GLB1):c.956-14T>CMucopolysaccharidosis, MPS-IV-B [RCV002903133]likely benign33304624633046246Human1name
155925185CV2099524single nucleotide variantNM_000404.4(GLB1):c.1144-4T>CMucopolysaccharidosis, MPS-IV-B [RCV002903535]likely benign33302165933021659Human1name
155941406CV2142967single nucleotide variantNM_000404.4(GLB1):c.552+19A>GMucopolysaccharidosis, MPS-IV-B [RCV002994077]likely benign33306544433065444Human1name
11551704CV251096single nucleotide variantNM_000404.4(GLB1):c.733+42T>Anot specified [RCV000253375]likely benign33305804733058047Humanname
401720383CV2737231single nucleotide variantNM_000404.4(GLB1):c.1347+1G>AGLB1-related disorder [RCV003314170]likely pathogenic33301844733018447Humanname , trait
11586965CV290779single nucleotide variantNM_000404.4(GLB1):c.1480-8C>GGM1 gangliosidosis [RCV000376709]|Mucopolysaccharidosis, MPS-IV-B [RCV000291569]|Mucopolysaccharidosis, MPS-IV-B [RCV000875356]likely benign|uncertain significance33301431833014318Human2name
405029426CV3082562single nucleotide variantNM_000404.4(GLB1):c.914+17T>CMucopolysaccharidosis, MPS-IV-B [RCV003786013]likely benign33305186633051866Human1name
405005547CV3082757deletionNM_000404.4(GLB1):c.458-13delMucopolysaccharidosis, MPS-IV-B [RCV003783856]benign33306557033065570Human1name
404989428CV3084089single nucleotide variantNM_000404.4(GLB1):c.734-11A>GMucopolysaccharidosis, MPS-IV-B [RCV003782281]likely benign33305356033053560Human1name
405024992CV3085123single nucleotide variantNM_000404.4(GLB1):c.1234-1G>TMucopolysaccharidosis, MPS-IV-B [RCV003795989]likely pathogenic33301856233018562Human1name
404995198CV3085350single nucleotide variantNM_000404.4(GLB1):c.734-14C>TMucopolysaccharidosis, MPS-IV-B [RCV003782881]likely benign33305356333053563Human1name
402524326CV3086726single nucleotide variantNM_000404.4(GLB1):c.245+16T>CMucopolysaccharidosis, MPS-IV-B [RCV003781343]likely benign33307252833072528Human1name
404984172CV3087219single nucleotide variantNM_000404.4(GLB1):c.553-20T>CMucopolysaccharidosis, MPS-IV-B [RCV003781682]likely benign33305828933058289Human1name
404984601CV3087280single nucleotide variantNM_000404.4(GLB1):c.396+14G>TMucopolysaccharidosis, MPS-IV-B [RCV003781743]likely benign33306880633068806Human1name
402512444CV3087392single nucleotide variantNM_000404.4(GLB1):c.458-14T>AMucopolysaccharidosis, MPS-IV-B [RCV003789743]likely benign33306557133065571Human1name
402513596CV3087432single nucleotide variantNM_000404.4(GLB1):c.792+16G>CMucopolysaccharidosis, MPS-IV-B [RCV003789783]likely benign33305347533053475Human1name
405019470CV3087895single nucleotide variantNM_000404.4(GLB1):c.733+11G>AMucopolysaccharidosis, MPS-IV-B [RCV003795455]likely benign33305807833058078Human1name
402522742CV3088254single nucleotide variantNM_000404.4(GLB1):c.246-13T>CMucopolysaccharidosis, MPS-IV-B [RCV003790590]likely benign33306898333068983Human1name
404997736CV3088635single nucleotide variantNM_000404.4(GLB1):c.793-13T>GMucopolysaccharidosis, MPS-IV-B [RCV003793413]likely benign33305201733052017Human1name
402508355CV3088792single nucleotide variantNM_000404.4(GLB1):c.733+20G>AMucopolysaccharidosis, MPS-IV-B [RCV003779996]likely benign33305806933058069Human1name
402510699CV3089243single nucleotide variantNM_000404.4(GLB1):c.1234-8C>TMucopolysaccharidosis, MPS-IV-B [RCV003780275]likely benign33301856933018569Human1name
402490677CV3090998single nucleotide variantNM_000404.4(GLB1):c.457+12C>AMucopolysaccharidosis, MPS-IV-B [RCV003787501]likely benign33306821833068218Human1name
404992712CV3091436single nucleotide variantNM_000404.4(GLB1):c.552+13T>AMucopolysaccharidosis, MPS-IV-B [RCV003792911]likely benign33306545033065450Human1name
402518550CV3091758single nucleotide variantNM_000404.4(GLB1):c.457+20T>CMucopolysaccharidosis, MPS-IV-B [RCV003790204]likely benign33306821033068210Human1name
402518762CV3091806single nucleotide variantNM_000404.4(GLB1):c.956-19G>AMucopolysaccharidosis, MPS-IV-B [RCV003790252]likely benign33304625133046251Human1name
402520674CV3091953single nucleotide variantNM_000404.4(GLB1):c.956-19G>TMucopolysaccharidosis, MPS-IV-B [RCV003790399]likely benign33304625133046251Human1name
402495691CV3092440single nucleotide variantNM_000404.4(GLB1):c.457+15A>GMucopolysaccharidosis, MPS-IV-B [RCV003788060]likely benign33306821533068215Human1name
405030213CV3092565single nucleotide variantNM_000404.4(GLB1):c.914+18G>TMucopolysaccharidosis, MPS-IV-B [RCV003786076]likely benign33305186533051865Human1name
405035748CV3093182single nucleotide variantNM_000404.4(GLB1):c.734-17C>TMucopolysaccharidosis, MPS-IV-B [RCV003786533]likely benign33305356633053566Human1name
405019589CV3094469single nucleotide variantNM_000404.4(GLB1):c.396+20G>AMucopolysaccharidosis, MPS-IV-B [RCV003785159]likely benign33306880033068800Human1name
404990836CV3094703single nucleotide variantNM_000404.4(GLB1):c.955+14A>CMucopolysaccharidosis, MPS-IV-B [RCV003792717]likely benign33305174433051744Human1name
405028149CV3094855single nucleotide variantNM_000404.4(GLB1):c.1347+9C>AMucopolysaccharidosis, MPS-IV-B [RCV003796217]likely benign33301843933018439Human1name
405053375CV3094922single nucleotide variantNM_000404.4(GLB1):c.734-16C>TMucopolysaccharidosis, MPS-IV-B [RCV003798236]likely benign33305356533053565Human1name
405054772CV3095035single nucleotide variantNM_000404.4(GLB1):c.396+15A>GMucopolysaccharidosis, MPS-IV-B [RCV003798349]likely benign33306880533068805Human1name
405002624CV3095604duplicationNM_000404.4(GLB1):c.734-11dupMucopolysaccharidosis, MPS-IV-B [RCV003793909]likely benign33305355933053560Human1name
405005359CV3096014single nucleotide variantNM_000404.4(GLB1):c.246-18C>TMucopolysaccharidosis, MPS-IV-B [RCV003794164]likely benign33306898833068988Human1name
405007675CV3096200single nucleotide variantNM_000404.4(GLB1):c.245+13G>AMucopolysaccharidosis, MPS-IV-B [RCV003794350]likely benign33307253133072531Human1name
405051589CV3097883single nucleotide variantNM_000404.4(GLB1):c.457+14G>AMucopolysaccharidosis, MPS-IV-B [RCV003808296]likely benign33306821633068216Human1name
405027846CV3098122single nucleotide variantNM_000404.4(GLB1):c.458-13T>CMucopolysaccharidosis, MPS-IV-B [RCV003806415]likely benign33306557033065570Human1name
404999615CV3099180single nucleotide variantNM_000404.4(GLB1):c.1069-8G>AMucopolysaccharidosis, MPS-IV-B [RCV003793601]likely benign33302433333024333Human1name
405020981CV3101257single nucleotide variantNM_000404.4(GLB1):c.246-16G>CMucopolysaccharidosis, MPS-IV-B [RCV003805836]likely benign33306898633068986Human1name
405002604CV3102090duplicationNM_000404.4(GLB1):c.457+11dupMucopolysaccharidosis, MPS-IV-B [RCV003804135]likely benign33306821833068219Human1name
405039179CV3103262single nucleotide variantNM_000404.4(GLB1):c.245+19G>TMucopolysaccharidosis, MPS-IV-B [RCV003797139]likely benign33307252533072525Human1name
405067977CV3103505single nucleotide variantNM_000404.4(GLB1):c.246-20G>AMucopolysaccharidosis, MPS-IV-B [RCV003799335]likely benign33306899033068990Human1name
405172908CV3104702single nucleotide variantNM_000404.4(GLB1):c.245+19G>AMucopolysaccharidosis, MPS-IV-B [RCV003803200]likely benign33307252533072525Human1name
405093072CV3105203single nucleotide variantNM_000404.4(GLB1):c.1479+7C>TMucopolysaccharidosis, MPS-IV-B [RCV003801086]likely benign33301670233016702Human1name
405062512CV3105371single nucleotide variantNM_000404.4(GLB1):c.734-10C>TMucopolysaccharidosis, MPS-IV-B [RCV003809135]likely benign33305355933053559Human1name
405093230CV3105442single nucleotide variantNM_000404.4(GLB1):c.733+10T>CMucopolysaccharidosis, MPS-IV-B [RCV003801158]likely benign33305807933058079Human1name
405081947CV3107441single nucleotide variantNM_000404.4(GLB1):c.1347+7A>GMucopolysaccharidosis, MPS-IV-B [RCV003800311]likely benign33301844133018441Human1name
405055025CV3107848single nucleotide variantNM_000404.4(GLB1):c.734-14C>GMucopolysaccharidosis, MPS-IV-B [RCV003808593]likely benign33305356333053563Human1name
405059866CV3108349single nucleotide variantNM_000404.4(GLB1):c.915-14T>CMucopolysaccharidosis, MPS-IV-B [RCV003808927]likely benign33305181233051812Human1name
405060381CV3108390single nucleotide variantNM_000404.4(GLB1):c.915-18T>CMucopolysaccharidosis, MPS-IV-B [RCV003808968]likely benign33305181633051816Human1name
405036268CV3108643single nucleotide variantNM_000404.4(GLB1):c.397-17T>CMucopolysaccharidosis, MPS-IV-B [RCV003807101]likely benign33306830733068307Human1name
405036964CV3108702single nucleotide variantNM_000404.4(GLB1):c.915-11T>GMucopolysaccharidosis, MPS-IV-B [RCV003807160]likely benign33305180933051809Human1name
405161122CV3109848single nucleotide variantNM_000404.4(GLB1):c.246-20G>CMucopolysaccharidosis, MPS-IV-B [RCV003802207]likely benign33306899033068990Human1name
405110903CV3110719single nucleotide variantNM_000404.4(GLB1):c.1348-7C>GMucopolysaccharidosis, MPS-IV-B [RCV003813622]likely benign33301684733016847Human1name
405155516CV3111309single nucleotide variantNM_000404.4(GLB1):c.246-10G>AMucopolysaccharidosis, MPS-IV-B [RCV003801765]likely benign33306898033068980Human1name
405108542CV3112334single nucleotide variantNM_000404.4(GLB1):c.245+10A>TMucopolysaccharidosis, MPS-IV-B [RCV003813177]likely benign33307253433072534Human1name
405107616CV3113846duplicationNM_000404.4(GLB1):c.1348-5dupMucopolysaccharidosis, MPS-IV-B [RCV003812969]benign33301684433016845Human1name
405691824CV3227598single nucleotide variantNM_000404.4(GLB1):c.1068+1G>TInfantile GM1 gangliosidosis [RCV003991944]uncertain significance33304611933046119Human1name , alternate_id
597896884CV3866117single nucleotide variantNM_000404.4(GLB1):c.955+10C>TMucopolysaccharidosis, MPS-IV-B [RCV005219734]likely benign33305174833051748Human1name
597866462CV3868924deletionNM_000404.4(GLB1):c.915-18delMucopolysaccharidosis, MPS-IV-B [RCV005215045]likely benign33305181633051816Human1name
597881271CV3869104single nucleotide variantNM_000404.4(GLB1):c.397-10C>TMucopolysaccharidosis, MPS-IV-B [RCV005217360]likely benign33306830033068300Human1name
597881497CV3869136single nucleotide variantNM_000404.4(GLB1):c.396+18G>TMucopolysaccharidosis, MPS-IV-B [RCV005217392]likely benign33306880233068802Human1name
597848995CV3872902single nucleotide variantNM_000404.4(GLB1):c.396+10G>TMucopolysaccharidosis, MPS-IV-B [RCV005212539]likely benign33306881033068810Human1name
597911410CV3879530single nucleotide variantNM_000404.4(GLB1):c.1068+4G>AMucopolysaccharidosis, MPS-IV-B [RCV005221931]uncertain significance33304611633046116Human1name
597912980CV3879761single nucleotide variantNM_000404.4(GLB1):c.1143+1G>TMucopolysaccharidosis, MPS-IV-B [RCV005222162]likely pathogenic33302425033024250Human1name
597914093CV3880083single nucleotide variantNM_000404.4(GLB1):c.792+18G>CMucopolysaccharidosis, MPS-IV-B [RCV005222322]likely benign33305347333053473Human1name
13517037CV488253single nucleotide variantNM_000404.4(GLB1):c.552+21G>Anot provided [RCV001549772]|not specified [RCV000596258]benign|likely benign33306544233065442Humanname
13787220CV542937single nucleotide variantNM_000404.4(GLB1):c.1144-2A>GGM1 gangliosidosis type 2 [RCV000673337]|Mucopolysaccharidosis, MPS-IV-B [RCV001071947]|Mucopolysaccharidosis, MPS-IV-B [RCV003387908]pathogenic|likely pathogenic33302165733021657Human2name , alternate_id
13788192CV543181single nucleotide variantNM_000404.4(GLB1):c.1479+1G>AGM1 gangliosidosis type 2 [RCV000673840]|Mucopolysaccharidosis, MPS-IV-B [RCV001389790]|not provided [RCV000731323]pathogenic|likely pathogenic33301670833016708Human2name , alternate_id
13785786CV543185single nucleotide variantNM_000404.4(GLB1):c.1233+1G>AGLB1-related disorder [RCV004723054]|GM1 gangliosidosis type 2 [RCV000672279]|Mucopolysaccharidosis, MPS-IV-B [RCV001855576]pathogenic|likely pathogenic33302156533021565Human5name , alternate_id
13787027CV549549single nucleotide variantNM_000404.4(GLB1):c.793-19C>TMucopolysaccharidosis, MPS-IV-B [RCV002060833]|not provided [RCV000675682]benign33305202333052023Human1name
14734746CV659781single nucleotide variantNM_000404.4(GLB1):c.955+60A>GInfantile GM1 gangliosidosis [RCV001527558]|Mucopolysaccharidosis, MPS-IV-B [RCV001527559]|not provided [RCV000837695]benign33305169833051698Human2name , alternate_id
15134688CV774802single nucleotide variantNM_000404.4(GLB1):c.1144-8C>GMucopolysaccharidosis, MPS-IV-B [RCV000942789]likely benign33302166333021663Human1name
28878051CV891636single nucleotide variantNM_000404.4(GLB1):c.1348-7C>TGM1 gangliosidosis [RCV001148554]|Mucopolysaccharidosis, MPS-IV-B [RCV001148555]|Mucopolysaccharidosis, MPS-IV-B [RCV001501788]likely benign|uncertain significance33301684733016847Human2name
28903328CV891637single nucleotide variantNM_000404.4(GLB1):c.1069-4A>GGM1 gangliosidosis [RCV001143991]|Mucopolysaccharidosis, MPS-IV-B [RCV001143992]|Mucopolysaccharidosis, MPS-IV-B [RCV001414861]likely benign|uncertain significance33302432933024329Human2name
38456574CV940747single nucleotide variantNM_000404.4(GLB1):c.1348-3C>GMucopolysaccharidosis, MPS-IV-B [RCV001217817]likely pathogenic|uncertain significance33301684333016843Human1name
8639818CV98801single nucleotide variantNM_000404.4(GLB1):c.1233+8T>CGM1 gangliosidosis [RCV000300510]|Infantile GM1 gangliosidosis [RCV001527524]|Mucopolysaccharidosis, MPS-IV-B [RCV000353081]|Mucopolysaccharidosis, MPS-IV-B [RCV001516016]|not provided [RCV000675680]|not specified [RCV000078700]benign|likely benign33302155833021558Human3name , alternate_id
8639833CV98816single nucleotide variantNM_000404.4(GLB1):c.458-11T>CGM1 gangliosidosis [RCV000330647]|Infantile GM1 gangliosidosis [RCV001527569]|Mucopolysaccharidosis, MPS-IV-B [RCV000278028]|Mucopolysaccharidosis, MPS-IV-B [RCV001518642]|not provided [RCV000675684]|not specified [RCV000078716]benign|likely benign33306556833065568Human3name , alternate_id
8639838CV98821single nucleotide variantNM_000404.4(GLB1):c.792+10G>TGM1 gangliosidosis [RCV000361060]|Infantile GM1 gangliosidosis [RCV001527560]|Mucopolysaccharidosis, MPS-IV-B [RCV000264041]|Mucopolysaccharidosis, MPS-IV-B [RCV001522843]|not provided [RCV000675683]|not specified [RCV000078722]benign|likely benign33305348133053481Human3name , alternate_id
127290157CV1113897single nucleotide variantNM_000404.4(GLB1):c.1735-10C>TMucopolysaccharidosis, MPS-IV-B [RCV001451132]likely benign33299735432997354Human1name
127330284CV1134791single nucleotide variantNM_000404.4(GLB1):c.1234-10T>GMucopolysaccharidosis, MPS-IV-B [RCV001488010]likely benign33301857133018571Human1name
127287625CV1163123single nucleotide variantNM_000404.4(GLB1):c.1233+91G>CInfantile GM1 gangliosidosis [RCV001527522]|Mucopolysaccharidosis, MPS-IV-B [RCV001527523]likely benign33302147533021475Human2name , alternate_id
127287686CV1163126single nucleotide variantNM_000404.4(GLB1):c.734-112T>CInfantile GM1 gangliosidosis [RCV001527565]|Mucopolysaccharidosis, MPS-IV-B [RCV001527566]|not provided [RCV001615230]benign33305366133053661Human2name , alternate_id
127287692CV1163128single nucleotide variantNM_000404.4(GLB1):c.76-4426C>TInfantile GM1 gangliosidosis [RCV001527570]|Mucopolysaccharidosis, MPS-IV-B [RCV001527571]|not provided [RCV001647357]benign33307713933077139Human2name , alternate_id
150408763CV1176313single nucleotide variantNM_000404.4(GLB1):c.955+300G>Anot provided [RCV001546014]likely benign33305145833051458Human3name
150408763CV1176313single nucleotide variantNM_000404.4(GLB1):c.955+300G>Anot provided [RCV001546014]likely benign33305145833051459Human3name
150416222CV1179692single nucleotide variantNM_000404.4(GLB1):c.792+187C>Gnot provided [RCV001549499]likely benign33305330433053304Humanname
150424281CV1183322deletionNM_000404.4(GLB1):c.734-116delnot provided [RCV001556456]likely benign33305366533053665Humanname
150429047CV1186577single nucleotide variantNM_000404.4(GLB1):c.1233+36A>Gnot provided [RCV001563078]likely benign33302153033021530Humanname
150429259CV1186578single nucleotide variantNM_000404.4(GLB1):c.1143+47G>Anot provided [RCV001563360]likely benign33302420433024204Humanname
150429360CV1186579single nucleotide variantNM_000404.4(GLB1):c.793-246A>Gnot provided [RCV001563495]likely benign33305225033052250Humanname
150419560CV1193295single nucleotide variantNM_000404.4(GLB1):c.246-140G>Anot provided [RCV001569738]likely benign33306911033069110Humanname
150421392CV1193296single nucleotide variantNM_000404.4(GLB1):c.245+141A>Tnot provided [RCV001570528]likely benign33307240333072403Humanname
150416535CV1197073single nucleotide variantNM_000404.4(GLB1):c.955+206A>Gnot provided [RCV001575920]likely benign33305155233051552Humanname
150513856CV1210734single nucleotide variantNM_000404.4(GLB1):c.76-4746T>Cnot provided [RCV001598775]benign33307745933077459Humanname
150510490CV1211731single nucleotide variantNM_000404.4(GLB1):c.246-252A>Cnot provided [RCV001597626]benign33306922233069222Humanname
150455900CV1220527single nucleotide variantNM_000404.4(GLB1):c.793-185C>Gnot provided [RCV001612620]benign33305218933052189Humanname
150439892CV1221373deletionNM_000404.4(GLB1):c.955+154delnot provided [RCV001610068]benign33305160433051604Humanname
150517274CV1226722single nucleotide variantNM_000404.4(GLB1):c.1480-74C>Gnot provided [RCV001639816]benign33301438433014384Humanname
150430099CV1231974single nucleotide variantNM_000404.4(GLB1):c.955+144T>Cnot provided [RCV001641236]benign33305161433051614Humanname
150504302CV1240727duplicationNM_000404.4(GLB1):c.955+123dupnot provided [RCV001657570]benign33305162633051627Humanname
150476806CV1251919single nucleotide variantNM_000404.4(GLB1):c.792+250G>Cnot provided [RCV001672118]benign33305324133053241Humanname
150485839CV1262177duplicationNM_000404.4(GLB1):c.955+139dupnot provided [RCV001686868]benign33305160333051604Humanname
150439844CV1266832single nucleotide variantNM_000404.4(GLB1):c.956-190C>Gnot provided [RCV001690267]benign33304642233046422Humanname
150467977CV1269321single nucleotide variantNM_000404.4(GLB1):c.956-118G>Cnot provided [RCV001694729]benign33304635033046350Humanname
150470468CV1269850single nucleotide variantNM_000404.4(GLB1):c.457+283T>Cnot provided [RCV001695137]benign33306794733067947Humanname
150477655CV1272077single nucleotide variantNM_000404.4(GLB1):c.792+231G>Anot provided [RCV001696363]benign33305326033053260Humanname
150463960CV1276302single nucleotide variantNM_000404.4(GLB1):c.457+154C>Tnot provided [RCV001710247]benign33306807633068076Humanname
152114837CV1537415single nucleotide variantNM_000404.4(GLB1):c.1068+20T>CMucopolysaccharidosis, MPS-IV-B [RCV002134962]likely benign33304610033046100Human1name
152155694CV1560999single nucleotide variantNM_000404.4(GLB1):c.1234-17A>TMucopolysaccharidosis, MPS-IV-B [RCV002102894]benign33301857833018578Human1name
152113030CV1585849duplicationNM_000404.4(GLB1):c.1143+14dupMucopolysaccharidosis, MPS-IV-B [RCV002153307]benign33302423633024237Human1name
152053881CV1595997single nucleotide variantNM_000404.4(GLB1):c.1348-16G>AMucopolysaccharidosis, MPS-IV-B [RCV002072702]likely benign33301685633016856Human1name
152093556CV1631970deletionNM_000404.4(GLB1):c.1143+14delMucopolysaccharidosis, MPS-IV-B [RCV002132340]benign33302423733024237Human1name
152135753CV1634499single nucleotide variantNM_000404.4(GLB1):c.1735-16G>CMucopolysaccharidosis, MPS-IV-B [RCV002218691]likely benign33299736032997360Human1name
156198614CV1886089single nucleotide variantNM_000404.4(GLB1):c.1735-12C>GMucopolysaccharidosis, MPS-IV-B [RCV003084134]likely benign33299735632997356Human1name
156039555CV1890926single nucleotide variantNM_000404.4(GLB1):c.1233+15G>AMucopolysaccharidosis, MPS-IV-B [RCV003078459]uncertain significance33302155133021551Human1name
156023833CV1895870single nucleotide variantNM_000404.4(GLB1):c.1233+19T>CMucopolysaccharidosis, MPS-IV-B [RCV003100329]likely benign33302154733021547Human1name
156025589CV1896188single nucleotide variantNM_000404.4(GLB1):c.1734+14T>CMucopolysaccharidosis, MPS-IV-B [RCV003100410]likely benign33301404233014042Human1name
156210324CV2032252single nucleotide variantNM_000404.4(GLB1):c.1068+18G>TMucopolysaccharidosis, MPS-IV-B [RCV002711739]likely benign33304610233046102Human1name
156067503CV2054576deletionNM_000404.4(GLB1):c.69_75+1delMucopolysaccharidosis, MPS-IV-B [RCV002797298]pathogenic33309701033097017Human1name
156112501CV2058318single nucleotide variantNM_000404.4(GLB1):c.1347+14C>TMucopolysaccharidosis, MPS-IV-B [RCV002824979]likely benign33301843433018434Human1name
155916807CV2091811deletionNM_000404.4(GLB1):c.1143+15delMucopolysaccharidosis, MPS-IV-B [RCV002903135]likely benign33302423633024236Human1name
156229085CV2093714single nucleotide variantNM_000404.4(GLB1):c.1234-20T>GMucopolysaccharidosis, MPS-IV-B [RCV002894484]likely benign33301858133018581Human1name
155928660CV2095883single nucleotide variantNM_000404.4(GLB1):c.1069-19T>CMucopolysaccharidosis, MPS-IV-B [RCV002903705]likely benign33302434433024344Human1name
156319365CV2111881single nucleotide variantNM_000404.4(GLB1):c.1234-19T>AMucopolysaccharidosis, MPS-IV-B [RCV002937648]likely benign33301858033018580Human1name
156068275CV2167097single nucleotide variantNM_000404.4(GLB1):c.1144-12G>AMucopolysaccharidosis, MPS-IV-B [RCV003019958]likely benign33302166733021667Human1name
155960447CV2183428deletionNM_000404.4(GLB1):c.1233+10delMucopolysaccharidosis, MPS-IV-B [RCV003032911]likely benign33302155633021556Human1name
401926292CV2827238single nucleotide variantNM_000404.4(GLB1):c.76-4429G>AGLB1-related disorder [RCV004540669]|not provided [RCV003437744]likely benign33307714233077142Humanname
401926294CV2827239single nucleotide variantNM_000404.4(GLB1):c.76-4483G>AGLB1-related disorder [RCV004540670]|not provided [RCV003437745]benign33307719633077196Humanname
11586502CV293941single nucleotide variantNM_000404.4(GLB1):c.1347+10G>AGLB1-related disorder [RCV004530391]|GM1 gangliosidosis [RCV000352478]|Mucopolysaccharidosis, MPS-IV-B [RCV000288195]|Mucopolysaccharidosis, MPS-IV-B [RCV000877602]likely benign|uncertain significance33301843833018438Human2name
11598676CV294406single nucleotide variantNM_000404.4(GLB1):c.1234-11T>AGM1 gangliosidosis [RCV000349673]|Mucopolysaccharidosis, MPS-IV-B [RCV000408323]|Mucopolysaccharidosis, MPS-IV-B [RCV002520118]likely benign|uncertain significance33301857233018572Human2name
405028643CV3082445single nucleotide variantNM_000404.4(GLB1):c.1347+13T>GMucopolysaccharidosis, MPS-IV-B [RCV003785896]likely benign33301843533018435Human1name
405028422CV3082504single nucleotide variantNM_000404.4(GLB1):c.1144-18G>CMucopolysaccharidosis, MPS-IV-B [RCV003785955]likely benign33302167333021673Human1name
405029004CV3082549single nucleotide variantNM_000404.4(GLB1):c.1734+13A>TMucopolysaccharidosis, MPS-IV-B [RCV003786000]likely benign33301404333014043Human1name
405048170CV3084351single nucleotide variantNM_000404.4(GLB1):c.1480-16T>CMucopolysaccharidosis, MPS-IV-B [RCV003797757]likely benign33301432633014326Human1name
405048158CV3084352single nucleotide variantNM_000404.4(GLB1):c.1347+19C>TMucopolysaccharidosis, MPS-IV-B [RCV003797758]likely benign33301842933018429Human1name
404997536CV3085729single nucleotide variantNM_000404.4(GLB1):c.1479+19T>CMucopolysaccharidosis, MPS-IV-B [RCV003783099]likely benign33301669033016690Human1name
404996944CV3088560single nucleotide variantNM_000404.4(GLB1):c.1734+13A>GMucopolysaccharidosis, MPS-IV-B [RCV003793337]likely benign33301404333014043Human1name
402510086CV3089188single nucleotide variantNM_000404.4(GLB1):c.1480-12T>GMucopolysaccharidosis, MPS-IV-B [RCV003780220]likely benign33301432233014322Human1name
402504014CV3090136single nucleotide variantNM_000404.4(GLB1):c.1479+17T>CMucopolysaccharidosis, MPS-IV-B [RCV003788903]likely benign33301669233016692Human1name
402498114CV3092843single nucleotide variantNM_000404.4(GLB1):c.1347+18A>CMucopolysaccharidosis, MPS-IV-B [RCV003788307]likely benign33301843033018430Human1name
405034163CV3093039single nucleotide variantNM_000404.4(GLB1):c.1068+14A>GMucopolysaccharidosis, MPS-IV-B [RCV003786390]likely benign33304610633046106Human1name
404990327CV3094653single nucleotide variantNM_000404.4(GLB1):c.1234-13C>AMucopolysaccharidosis, MPS-IV-B [RCV003792666]likely benign33301857433018574Human1name
405054315CV3094939deletionNM_000404.4(GLB1):c.1348-16delMucopolysaccharidosis, MPS-IV-B [RCV003798253]likely benign33301685633016856Human1name
405006425CV3096086single nucleotide variantNM_000404.4(GLB1):c.1479+13A>GMucopolysaccharidosis, MPS-IV-B [RCV003794236]likely benign33301669633016696Human1name
404988884CV3097130single nucleotide variantNM_000404.4(GLB1):c.1479+20C>GMucopolysaccharidosis, MPS-IV-B [RCV003792519]likely benign33301668933016689Human1name
405000097CV3099231single nucleotide variantNM_000404.4(GLB1):c.1069-20T>CMucopolysaccharidosis, MPS-IV-B [RCV003793652]likely benign33302434533024345Human1name
404980635CV3099623deletionNM_000404.4(GLB1):c.1233+15delMucopolysaccharidosis, MPS-IV-B [RCV003791452]likely benign33302155133021551Human1name
404982981CV3100166single nucleotide variantNM_000404.4(GLB1):c.1069-17T>GMucopolysaccharidosis, MPS-IV-B [RCV003791833]likely benign33302434233024342Human1name
404977368CV3102673single nucleotide variantNM_000404.4(GLB1):c.1347+20T>CMucopolysaccharidosis, MPS-IV-B [RCV003790767]likely benign33301842833018428Human1name
404977461CV3102692single nucleotide variantNM_000404.4(GLB1):c.1234-13C>GMucopolysaccharidosis, MPS-IV-B [RCV003790786]likely benign33301857433018574Human1name
405042481CV3103702single nucleotide variantNM_000404.4(GLB1):c.1143+11A>GMucopolysaccharidosis, MPS-IV-B [RCV003797420]likely benign33302424033024240Human1name
405015550CV3104462single nucleotide variantNM_000404.4(GLB1):c.1068+18G>CMucopolysaccharidosis, MPS-IV-B [RCV003805331]likely benign33304610233046102Human1name
405014885CV3106676single nucleotide variantNM_000404.4(GLB1):c.1143+16A>TMucopolysaccharidosis, MPS-IV-B [RCV003795013]likely benign33302423533024235Human1name
405061869CV3108534single nucleotide variantNM_000404.4(GLB1):c.1068+18G>AMucopolysaccharidosis, MPS-IV-B [RCV003809112]likely benign33304610233046102Human1name
405110849CV3110686single nucleotide variantNM_000404.4(GLB1):c.1233+12A>GMucopolysaccharidosis, MPS-IV-B [RCV003813589]likely benign33302155433021554Human1name
405107501CV3113818single nucleotide variantNM_000404.4(GLB1):c.1233+13A>CMucopolysaccharidosis, MPS-IV-B [RCV003812941]likely benign33302155333021553Human1name
405282445CV3191014single nucleotide variantNM_000404.4(GLB1):c.76-4414C>TGLB1-related disorder [RCV004537118]likely benign33307712733077127Humanname , trait
405293059CV3207216single nucleotide variantNM_000404.4(GLB1):c.76-4376G>AGLB1-related disorder [RCV004539491]benign|likely benign33307708933077089Humanname , trait
405278241CV3216456single nucleotide variantNM_000404.4(GLB1):c.76-4520G>AGLB1-related disorder [RCV004544135]benign33307723333077233Humanname , trait
597841423CV3868267single nucleotide variantNM_000404.4(GLB1):c.1347+16G>CMucopolysaccharidosis, MPS-IV-B [RCV005211300]likely benign33301843233018432Human1name
597862232CV3875185single nucleotide variantNM_000404.4(GLB1):c.1347+12C>TMucopolysaccharidosis, MPS-IV-B [RCV005214362]likely benign33301843633018436Human1name
13784671CV543224deletionNM_000404.4(GLB1):c.65_75+1delGM1 gangliosidosis type 2 [RCV000671128]|Infantile GM1 gangliosidosis [RCV003155274]|Mucopolysaccharidosis, MPS-IV-B [RCV001861803]|not provided [RCV001784268]pathogenic|likely pathogenic33309701033097021Human3name , alternate_id
13787023CV549548single nucleotide variantNM_000404.4(GLB1):c.1143+28G>Cnot provided [RCV000675681]likely benign33302422333024223Humanname
14734238CV659724single nucleotide variantNM_000404.4(GLB1):c.553-119A>Gnot provided [RCV000837463]benign33305838833058388Humanname
14734624CV659883single nucleotide variantNM_000404.4(GLB1):c.396+122C>Anot provided [RCV000837640]benign33306869833068698Humanname
14734743CV659984single nucleotide variantNM_000404.4(GLB1):c.793-132T>Gnot provided [RCV000837694]benign33305213633052136Humanname
14735598CV659990single nucleotide variantNM_000404.4(GLB1):c.457+235A>Gnot provided [RCV000838084]benign33306799533067995Humanname
14734621CV659991single nucleotide variantNM_000404.4(GLB1):c.246-194A>Gnot provided [RCV000837639]benign33306916433069164Humanname
15168073CV777248single nucleotide variantNM_000404.4(GLB1):c.1735-10C>GMucopolysaccharidosis, MPS-IV-B [RCV000949183]likely benign33299735432997354Human1name
28878045CV891635single nucleotide variantNM_000404.4(GLB1):c.1479+11C>TGM1 gangliosidosis [RCV001148553]|Mucopolysaccharidosis, MPS-IV-B [RCV001148552]|Mucopolysaccharidosis, MPS-IV-B [RCV002070801]likely benign|uncertain significance33301669833016698Human2name
150405024CV1176311single nucleotide variantNM_000404.4(GLB1):c.1734+169G>Anot provided [RCV001544675]likely benign33301388733013887Humanname
150415591CV1176312single nucleotide variantNM_000404.4(GLB1):c.1068+291A>Cnot provided [RCV001548648]likely benign33304582933045829Humanname
150435038CV1206897single nucleotide variantNM_000404.4(GLB1):c.1480-295A>Gnot provided [RCV001582246]likely benign33301460533014605Humanname
150491653CV1210400single nucleotide variantNM_000404.4(GLB1):c.1234-307G>Anot provided [RCV001592682]likely benign33301886833018868Humanname
150510870CV1210604single nucleotide variantNM_000404.4(GLB1):c.1480-272T>Cnot provided [RCV001597783]benign33301458233014582Humanname
150512061CV1212906single nucleotide variantNM_000404.4(GLB1):c.1480-320C>Anot provided [RCV001598138]benign33301463033014630Humanname
150470131CV1219190single nucleotide variantNM_000404.4(GLB1):c.1734+233C>Tnot provided [RCV001614942]benign33301382333013823Humanname
150455473CV1220465single nucleotide variantNM_000404.4(GLB1):c.1068+217G>Tnot provided [RCV001612558]benign33304590333045903Humanname
150482475CV1221059single nucleotide variantNM_000404.4(GLB1):c.1347+208A>Gnot provided [RCV001617144]benign33301824033018240Humanname
150499526CV1224605single nucleotide variantNM_000404.4(GLB1):c.1069-231G>Anot provided [RCV001620436]benign33302455633024556Humanname
150431134CV1235346single nucleotide variantNM_000404.4(GLB1):c.1347+194G>Tnot provided [RCV001641716]benign33301825433018254Humanname
150489392CV1236357single nucleotide variantNM_000404.4(GLB1):c.1068+264G>Anot provided [RCV001654498]benign33304585633045856Humanname
150456112CV1236841single nucleotide variantNM_000404.4(GLB1):c.1234-177C>Tnot provided [RCV001648577]benign33301873833018738Humanname
150488234CV1237448single nucleotide variantNM_000404.4(GLB1):c.1479+204A>Gnot provided [RCV001654297]benign33301650533016505Humanname
150477473CV1240035single nucleotide variantNM_000404.4(GLB1):c.1480-149T>Cnot provided [RCV001652213]benign33301445933014459Humanname
150472136CV1270206single nucleotide variantNM_000404.4(GLB1):c.1233+174G>Tnot provided [RCV001695494]benign33302139233021392Humanname
150490791CV1279969single nucleotide variantNM_000404.4(GLB1):c.1144-256C>Gnot provided [RCV001716534]benign33302191133021911Humanname
150471655CV1281039single nucleotide variantNM_000404.4(GLB1):c.1734+188C>Tnot provided [RCV001713230]benign33301386833013868Humanname
150444580CV1288043single nucleotide variantNM_000404.4(GLB1):c.1233+218C>Tnot provided [RCV001725765]benign33302134833021348Humanname
155989004CV2026823microsatelliteNM_000404.4(GLB1):c.246-16GT[2]GLB1-related disorder [RCV004545385]|Mucopolysaccharidosis, MPS-IV-B [RCV002755666]likely benign|uncertain significance33306897933068982Humanname
127251616CV1070683microsatelliteNM_000404.4(GLB1):c.1735-15TC[4]Mucopolysaccharidosis, MPS-IV-B [RCV001400149]likely benign33299734832997351Humanname
127283332CV1070684microsatelliteNM_000404.4(GLB1):c.1735-15TC[5]Mucopolysaccharidosis, MPS-IV-B [RCV001411711]likely benign33299734832997349Humanname
8555883CV15966duplicationNM_000404.2(GLB1):c.1069_1233dupInfantile GM1 gangliosidosis [RCV000000975]pathogenicHuman1name , alternate_id
155911858CV1935193deletionNM_000404.4(GLB1):c.75+3_75+4delInfantile GM1 gangliosidosis [RCV002510481]uncertain significance33309700733097008Human1name , alternate_id
11592941CV290017microsatelliteNM_000404.4(GLB1):c.1735-15TC[7]GM1 gangliosidosis [RCV000405716]|Morquio syndrome [RCV000343636]|Mucopolysaccharidosis, MPS-IV-B [RCV001419273]likely benign|uncertain significance33299734732997348Humanname
13786247CV543190deletionNM_000404.4(GLB1):c.769_792+13delGM1 gangliosidosis type 2 [RCV000672678]|Mucopolysaccharidosis, MPS-IV-B [RCV001043055]pathogenic|likely pathogenic33305347833053514Human2name , alternate_id
152137384CV1563389single nucleotide variantNM_000404.4(GLB1):c.9G>A (p.Gly3=)Mucopolysaccharidosis, MPS-IV-B [RCV002200127]likely benign33309707733097077Human1name
405047440CV3084402single nucleotide variantNM_000404.4(GLB1):c.6G>A (p.Pro2=)Mucopolysaccharidosis, MPS-IV-B [RCV003797808]likely benign33309708033097080Human1name
597861047CV3865296single nucleotide variantNM_000404.4(GLB1):c.9G>C (p.Gly3=)Mucopolysaccharidosis, MPS-IV-B [RCV005214190]likely benign33309707733097077Human1name
13788602CV543114deletionNM_000404.4(GLB1):c.733+2_733+4delGM1 gangliosidosis type 2 [RCV000674052]likely pathogenic33305808533058087Human1name , alternate_id
127305714CV1134802single nucleotide variantNM_000404.4(GLB1):c.27C>T (p.Leu9=)Mucopolysaccharidosis, MPS-IV-B [RCV001479824]likely benign33309705933097059Human1name
151351354CV1323497deletionNM_000404.4(GLB1):c.246-17_246-3delInfantile GM1 gangliosidosis [RCV001806353]likely pathogenic33306897333068987Human1name , alternate_id
152034726CV1639550single nucleotide variantNM_000404.4(GLB1):c.15G>T (p.Leu5=)Mucopolysaccharidosis, MPS-IV-B [RCV002187304]likely benign33309707133097071Human1name
155942674CV2039290single nucleotide variantNM_000404.4(GLB1):c.27C>G (p.Leu9=)Mucopolysaccharidosis, MPS-IV-B [RCV002775296]likely benign33309705933097059Human1name
405043480CV3103776single nucleotide variantNM_000404.4(GLB1):c.12C>T (p.Phe4=)Mucopolysaccharidosis, MPS-IV-B [RCV003797494]likely benign33309707433097074Human1name
127267519CV1092391single nucleotide variantNM_000404.4(GLB1):c.42T>C (p.Val14=)Mucopolysaccharidosis, MPS-IV-B [RCV001429728]likely benign33309704433097044Human1name
127283264CV1092392single nucleotide variantNM_000404.4(GLB1):c.31C>T (p.Leu11=)Mucopolysaccharidosis, MPS-IV-B [RCV001448423]likely benign33309705533097055Human1name
127307970CV1113918single nucleotide variantNM_000404.4(GLB1):c.66C>T (p.Arg22=)Mucopolysaccharidosis, MPS-IV-B [RCV001455939]likely benign33309702033097020Human1name
151799717CV1369756single nucleotide variantNM_000404.4(GLB1):c.69C>A (p.Gly23=)Mucopolysaccharidosis, MPS-IV-B [RCV001920776]likely benign33309701733097017Human1name
151714374CV1408801single nucleotide variantNM_000404.4(GLB1):c.4C>G (p.Pro2Ala)Mucopolysaccharidosis, MPS-IV-B [RCV002015648]uncertain significance33309708233097082Human1name
152084384CV1525475single nucleotide variantNM_000404.4(GLB1):c.63G>A (p.Thr21=)Mucopolysaccharidosis, MPS-IV-B [RCV002131238]likely benign33309702333097023Human1name
152124566CV1564171single nucleotide variantNM_000404.4(GLB1):c.78T>C (p.Asn26=)Mucopolysaccharidosis, MPS-IV-B [RCV002176018]likely benign33307271133072711Human1name
152042889CV1637600single nucleotide variantNM_000404.4(GLB1):c.84C>T (p.Thr28=)Mucopolysaccharidosis, MPS-IV-B [RCV002144734]likely benign33307270533072705Human1name
10047475CV190258single nucleotide variantNM_000404.4(GLB1):c.1A>C (p.Met1Leu)not provided [RCV000173126]likely pathogenic33309708533097085Humanname
156413330CV1904837single nucleotide variantNM_000404.4(GLB1):c.81C>T (p.Ala27=)Mucopolysaccharidosis, MPS-IV-B [RCV002588130]likely benign33307270833072708Human1name
156034899CV1932643single nucleotide variantNM_000404.4(GLB1):c.5C>T (p.Pro2Leu)Mucopolysaccharidosis, MPS-IV-B [RCV002637327]uncertain significance33309708133097081Human1name
156114821CV1952260single nucleotide variantNM_000404.4(GLB1):c.3G>A (p.Met1Ile)Infantile GM1 gangliosidosis [RCV002571631]likely pathogenic33309708333097083Human1name , alternate_id
156329630CV2065108single nucleotide variantNM_000404.4(GLB1):c.37C>T (p.Leu13=)Mucopolysaccharidosis, MPS-IV-B [RCV002835222]likely benign33309704933097049Human1name
11594724CV290021single nucleotide variantNM_000404.4(GLB1):c.4C>A (p.Pro2Thr)GM1 gangliosidosis [RCV000310011]|Inborn genetic diseases [RCV002520119]|Mucopolysaccharidosis, MPS-IV-B [RCV000362274]|Mucopolysaccharidosis, MPS-IV-B [RCV002520120]uncertain significance33309708233097082Human3name
405020650CV3101223single nucleotide variantNM_000404.4(GLB1):c.45G>C (p.Leu15=)Mucopolysaccharidosis, MPS-IV-B [RCV003805802]likely benign33309704133097041Human1name
405056549CV3102336single nucleotide variantNM_000404.4(GLB1):c.70T>C (p.Leu24=)Mucopolysaccharidosis, MPS-IV-B [RCV003798478]likely benign33309701633097016Human1name
405037869CV3106335single nucleotide variantNM_000404.4(GLB1):c.33G>C (p.Leu11=)Mucopolysaccharidosis, MPS-IV-B [RCV003797026]likely benign33309705333097053Human1name
597897998CV3875978single nucleotide variantNM_000404.4(GLB1):c.39G>A (p.Leu13=)Mucopolysaccharidosis, MPS-IV-B [RCV005219868]likely benign33309704733097047Human1name
15117268CV781643single nucleotide variantNM_000404.4(GLB1):c.69C>G (p.Gly23=)Mucopolysaccharidosis, MPS-IV-B [RCV001409590]likely benign33309701733097017Human1name
38469643CV953436single nucleotide variantNM_000404.4(GLB1):c.5C>G (p.Pro2Arg)Mucopolysaccharidosis, MPS-IV-B [RCV001248682]likely benign|uncertain significance33309708133097081Human1name
8639829CV98812single nucleotide variantNM_000404.4(GLB1):c.34T>C (p.Leu12=)GM1 gangliosidosis [RCV000302471]|GM1 gangliosidosis type 2 [RCV001701492]|GM1 gangliosidosis type 3 [RCV001701493]|Infantile GM1 gangliosidosis [RCV001527572]|Mucopolysaccharidosis, MPS-IV-B [RCV000392270]|Mucopolysaccharidosis, MPS-IV-B [RCV001518401]|not provided [RCV000675687]|not specified [RCVlikely pathogenic|benign|conflicting interpretations of pathogenicity|conflicting data from submitters33309705233097052Human5name , alternate_id
127284089CV1070686duplicationNM_000404.4(GLB1):c.1735-16_1735-9dupMucopolysaccharidosis, MPS-IV-B [RCV001412232]likely benign33299735232997353Human1name
127281676CV1070701single nucleotide variantNM_000404.4(GLB1):c.229C>T (p.Leu77=)Mucopolysaccharidosis, MPS-IV-B [RCV001410632]likely benign33307256033072560Human1name
127234165CV1070702single nucleotide variantNM_000404.4(GLB1):c.105C>T (p.Asp35=)Mucopolysaccharidosis, MPS-IV-B [RCV001396379]likely benign33307268433072684Human1name
127287825CV1113917single nucleotide variantNM_000404.4(GLB1):c.132T>C (p.Asp44=)Mucopolysaccharidosis, MPS-IV-B [RCV001450237]likely benign33307265733072657Human1name
127303044CV1134800single nucleotide variantNM_000404.4(GLB1):c.150C>T (p.Tyr50=)Mucopolysaccharidosis, MPS-IV-B [RCV001479134]likely benign33307263933072639Human1name
127322813CV1134801single nucleotide variantNM_000404.4(GLB1):c.123C>T (p.Phe41=)Mucopolysaccharidosis, MPS-IV-B [RCV001505229]likely benign33307266633072666Human1name
151808593CV1389548single nucleotide variantNM_000404.4(GLB1):c.20G>C (p.Arg7Pro)Mucopolysaccharidosis, MPS-IV-B [RCV001937147]uncertain significance33309706633097066Human1name
151797093CV1431319single nucleotide variantNM_000404.4(GLB1):c.270G>A (p.Glu90=)Mucopolysaccharidosis, MPS-IV-B [RCV001915028]likely benign33306894633068946Human1name
152097001CV1566151indelNM_000404.4(GLB1):c.76-9_76-8delinsAAMucopolysaccharidosis, MPS-IV-B [RCV002094981]likely benign33307272133072722Humanname
152121868CV1570329single nucleotide variantNM_000404.4(GLB1):c.138G>A (p.Gln46=)Mucopolysaccharidosis, MPS-IV-B [RCV002216890]likely benign33307265133072651Human1name
152109902CV1617569single nucleotide variantNM_000404.4(GLB1):c.141A>G (p.Pro47=)Mucopolysaccharidosis, MPS-IV-B [RCV002116414]likely benign33307264833072648Human1name
152074492CV1620405single nucleotide variantNM_000404.4(GLB1):c.228G>C (p.Gly76=)Mucopolysaccharidosis, MPS-IV-B [RCV002111910]likely benign33307256133072561Human1name
152084020CV1662903single nucleotide variantNM_000404.4(GLB1):c.192C>T (p.Tyr64=)Mucopolysaccharidosis, MPS-IV-B [RCV002170921]likely benign33307259733072597Human1name
152053127CV1665155single nucleotide variantNM_000404.4(GLB1):c.126C>G (p.Leu42=)Mucopolysaccharidosis, MPS-IV-B [RCV002089405]likely benign33307266333072663Human1name
156222367CV1934315single nucleotide variantNM_000404.4(GLB1):c.126C>A (p.Leu42=)Mucopolysaccharidosis, MPS-IV-B [RCV002644460]likely benign33307266333072663Human1name
156437320CV1937458single nucleotide variantNM_000404.4(GLB1):c.126C>T (p.Leu42=)Mucopolysaccharidosis, MPS-IV-B [RCV003106852]likely benign33307266333072663Human1name
155963874CV2080620single nucleotide variantNM_000404.4(GLB1):c.165T>C (p.Ile55=)Mucopolysaccharidosis, MPS-IV-B [RCV002862987]likely benign33307262433072624Human1name
155978913CV2166893single nucleotide variantNM_000404.4(GLB1):c.228G>A (p.Gly76=)Mucopolysaccharidosis, MPS-IV-B [RCV003033786]likely benign33307256133072561Human1name
156017211CV2177598single nucleotide variantNM_000404.4(GLB1):c.261C>T (p.Asn87=)Mucopolysaccharidosis, MPS-IV-B [RCV003035546]likely benign33306895533068955Human1name
11551291CV251092single nucleotide variantNM_000404.4(GLB1):c.1561= (p.Cys521=)Mucopolysaccharidosis, MPS-IV-B [RCV000548417]|not specified [RCV000252845]benign33301422933014229Human1name
11592793CV293942single nucleotide variantNM_000404.4(GLB1):c.234C>T (p.Asn78=)GM1 gangliosidosis [RCV000279897]|Mucopolysaccharidosis, MPS-IV-B [RCV000341987]|Mucopolysaccharidosis, MPS-IV-B [RCV000875466]likely benign|uncertain significance33307255533072555Human2name
405003678CV3086495single nucleotide variantNM_000404.4(GLB1):c.210G>A (p.Leu70=)Mucopolysaccharidosis, MPS-IV-B [RCV003783709]likely benign33307257933072579Human1name
404984886CV3087317single nucleotide variantNM_000404.4(GLB1):c.174C>G (p.Ser58=)Mucopolysaccharidosis, MPS-IV-B [RCV003781780]likely benign33307261533072615Human1name
405005941CV3095935single nucleotide variantNM_000404.4(GLB1):c.114G>A (p.Arg38=)Mucopolysaccharidosis, MPS-IV-B [RCV003794085]likely benign33307267533072675Human1name
405127203CV3112033single nucleotide variantNM_000404.4(GLB1):c.279A>G (p.Pro93=)Mucopolysaccharidosis, MPS-IV-B [RCV003815506]likely benign33306893733068937Human1name
597638583CV3717471deletionNM_000404.4(GLB1):c.47del (p.Leu16fs)GM1 gangliosidosis type 2 [RCV005024603]likely pathogenic33309703933097039Human1name , alternate_id
597638588CV3717472duplicationNM_000404.4(GLB1):c.29dup (p.Leu11fs)GM1 gangliosidosis type 2 [RCV005024604]likely pathogenic33309705633097057Human1name , alternate_id
597883490CV3866008single nucleotide variantNM_000404.4(GLB1):c.112C>A (p.Arg38=)Mucopolysaccharidosis, MPS-IV-B [RCV005217673]likely benign33307267733072677Human1name
15191530CV763822single nucleotide variantNM_000404.4(GLB1):c.204G>T (p.Arg68=)Mucopolysaccharidosis, MPS-IV-B [RCV001396744]likely benign33307258533072585Human1name
8639835CV98818duplicationNM_000404.4(GLB1):c.51dup (p.Leu18fs)Mucopolysaccharidosis, MPS-IV-B [RCV001854386]|not provided [RCV000173123]pathogenic33309703433097035Human1name
126913887CV1037351single nucleotide variantNM_000404.4(GLB1):c.486G>A (p.Leu162=)Mucopolysaccharidosis, MPS-IV-B [RCV002547671]|not provided [RCV001357779]likely benign|uncertain significance33306552933065529Human1name
127251158CV1070691single nucleotide variantNM_000404.4(GLB1):c.975A>G (p.Ala325=)Mucopolysaccharidosis, MPS-IV-B [RCV001417724]likely benign33304621333046213Human1name
127241453CV1070693single nucleotide variantNM_000404.4(GLB1):c.876C>G (p.Ser292=)Mucopolysaccharidosis, MPS-IV-B [RCV001393152]likely benign33305192133051921Human1name
127233262CV1070694single nucleotide variantNM_000404.4(GLB1):c.717G>T (p.Thr239=)Mucopolysaccharidosis, MPS-IV-B [RCV001396054]likely benign33305810533058105Human1name
127257386CV1070695single nucleotide variantNM_000404.4(GLB1):c.678A>G (p.Thr226=)Mucopolysaccharidosis, MPS-IV-B [RCV001401445]likely benign33305814433058144Human1name
127231475CV1070696single nucleotide variantNM_000404.4(GLB1):c.669A>G (p.Ala223=)Mucopolysaccharidosis, MPS-IV-B [RCV001395340]likely benign33305815333058153Human1name
127240619CV1070697single nucleotide variantNM_000404.4(GLB1):c.519C>G (p.Leu173=)Mucopolysaccharidosis, MPS-IV-B [RCV001397804]likely benign33306549633065496Human1name
127284100CV1070698single nucleotide variantNM_000404.4(GLB1):c.496C>T (p.Leu166=)Mucopolysaccharidosis, MPS-IV-B [RCV001412247]likely benign33306551933065519Human1name
127278070CV1070699single nucleotide variantNM_000404.4(GLB1):c.366C>T (p.Pro122=)Mucopolysaccharidosis, MPS-IV-B [RCV001408256]likely benign33306885033068850Human1name
127240436CV1070700single nucleotide variantNM_000404.4(GLB1):c.327G>T (p.Arg109=)Mucopolysaccharidosis, MPS-IV-B [RCV001397771]likely benign33306888933068889Human1name
127245243CV1092379single nucleotide variantNM_000404.4(GLB1):c.972T>C (p.Tyr324=)Mucopolysaccharidosis, MPS-IV-B [RCV001424269]likely benign33304621633046216Human1name
127243161CV1092381single nucleotide variantNM_000404.4(GLB1):c.948T>C (p.Tyr316=)Mucopolysaccharidosis, MPS-IV-B [RCV001434773]likely benign33305176533051765Human1name
127247493CV1092382single nucleotide variantNM_000404.4(GLB1):c.903G>A (p.Ala301=)Mucopolysaccharidosis, MPS-IV-B [RCV001424714]likely benign33305189433051894Human1name
127263350CV1092383single nucleotide variantNM_000404.4(GLB1):c.879C>T (p.Leu293=)Mucopolysaccharidosis, MPS-IV-B [RCV001439263]likely benign33305191833051918Human1name
127254552CV1092386single nucleotide variantNM_000404.4(GLB1):c.546A>G (p.Thr182=)Inborn genetic diseases [RCV004038237]|Mucopolysaccharidosis, MPS-IV-B [RCV001426326]likely benign33306546933065469Human2name
127265607CV1092387single nucleotide variantNM_000404.4(GLB1):c.336T>C (p.His112=)Mucopolysaccharidosis, MPS-IV-B [RCV001429140]likely benign33306888033068880Human1name
127246184CV1092390single nucleotide variantNM_000404.4(GLB1):c.61A>G (p.Thr21Ala)Inborn genetic diseases [RCV002555195]|Mucopolysaccharidosis, MPS-IV-B [RCV001435358]|not provided [RCV002261364]likely benign|uncertain significance33309702533097025Human2name
127314849CV1113907single nucleotide variantNM_000404.4(GLB1):c.993C>T (p.Tyr331=)Mucopolysaccharidosis, MPS-IV-B [RCV001457823]likely benign33304619533046195Human1name
127327261CV1113908single nucleotide variantNM_000404.4(GLB1):c.987C>T (p.Thr329=)Mucopolysaccharidosis, MPS-IV-B [RCV001469019]likely benign33304620133046201Human1name
127302759CV1113910single nucleotide variantNM_000404.4(GLB1):c.912C>T (p.Asn304=)Mucopolysaccharidosis, MPS-IV-B [RCV001461735]likely benign33305188533051885Human1name
127322709CV1113911single nucleotide variantNM_000404.4(GLB1):c.789C>G (p.Pro263=)Mucopolysaccharidosis, MPS-IV-B [RCV001467703]likely benign33305349433053494Human1name
127301179CV1113912single nucleotide variantNM_000404.4(GLB1):c.693G>T (p.Gly231=)Mucopolysaccharidosis, MPS-IV-B [RCV001461314]likely benign33305812933058129Human1name
127328690CV1113913single nucleotide variantNM_000404.4(GLB1):c.561T>C (p.Asn187=)Mucopolysaccharidosis, MPS-IV-B [RCV001469708]likely benign33305826133058261Human1name
127332048CV1113914single nucleotide variantNM_000404.4(GLB1):c.450C>T (p.Ser150=)Mucopolysaccharidosis, MPS-IV-B [RCV001471961]likely benign33306823733068237Human1name
127322744CV1113915single nucleotide variantNM_000404.4(GLB1):c.402A>T (p.Gly134=)Mucopolysaccharidosis, MPS-IV-B [RCV001467713]likely benign33306828533068285Human1name
127291484CV1113916single nucleotide variantNM_000404.4(GLB1):c.342G>A (p.Leu114=)Mucopolysaccharidosis, MPS-IV-B [RCV001476096]likely benign33306887433068874Human1name
127306517CV1134793single nucleotide variantNM_000404.4(GLB1):c.873C>T (p.Ser291=)Mucopolysaccharidosis, MPS-IV-B [RCV001500262]likely benign33305192433051924Human1name
127294549CV1134794single nucleotide variantNM_000404.4(GLB1):c.813T>C (p.Thr271=)Mucopolysaccharidosis, MPS-IV-B [RCV001497008]likely benign33305198433051984Human1name
127323926CV1134798single nucleotide variantNM_000404.4(GLB1):c.708C>T (p.Leu236=)Mucopolysaccharidosis, MPS-IV-B [RCV001485352]likely benign33305811433058114Human1name
127315639CV1134799single nucleotide variantNM_000404.4(GLB1):c.681C>T (p.Phe227=)GLB1-related disorder [RCV004533905]|Mucopolysaccharidosis, MPS-IV-B [RCV001502767]likely benign33305814133058141Human2name
151709029CV1359476single nucleotide variantNM_000404.4(GLB1):c.40G>C (p.Val14Leu)Mucopolysaccharidosis, MPS-IV-B [RCV001991878]|not provided [RCV004793685]uncertain significance33309704633097046Human1name
152074476CV1520944single nucleotide variantNM_000404.4(GLB1):c.315A>G (p.Glu105=)Mucopolysaccharidosis, MPS-IV-B [RCV002075540]likely benign33306890133068901Human1name
152043212CV1522360single nucleotide variantNM_000404.4(GLB1):c.837A>G (p.Gln279=)Mucopolysaccharidosis, MPS-IV-B [RCV002088230]likely benign33305196033051960Human1name
152112037CV1539176single nucleotide variantNM_000404.4(GLB1):c.624C>T (p.Arg208=)Mucopolysaccharidosis, MPS-IV-B [RCV002080384]likely benign33305819833058198Human1name
152063289CV1542316single nucleotide variantNM_000404.4(GLB1):c.366C>G (p.Pro122=)Mucopolysaccharidosis, MPS-IV-B [RCV002208964]likely benign33306885033068850Human1name
152143632CV1543012single nucleotide variantNM_000404.4(GLB1):c.312G>A (p.Val104=)Mucopolysaccharidosis, MPS-IV-B [RCV002178386]|not specified [RCV004587321]likely benign33306890433068904Human1name
152155265CV1560937single nucleotide variantNM_000404.4(GLB1):c.360G>A (p.Leu120=)Mucopolysaccharidosis, MPS-IV-B [RCV002102846]likely benign33306885633068856Human1name
152045630CV1561280single nucleotide variantNM_000404.4(GLB1):c.963C>T (p.Asn321=)Mucopolysaccharidosis, MPS-IV-B [RCV002108309]likely benign33304622533046225Human1name
152088291CV1562900single nucleotide variantNM_000404.4(GLB1):c.876C>T (p.Ser292=)Mucopolysaccharidosis, MPS-IV-B [RCV002113719]likely benign33305192133051921Human1name
152102329CV1571597single nucleotide variantNM_000404.4(GLB1):c.843C>T (p.His281=)Mucopolysaccharidosis, MPS-IV-B [RCV002173263]likely benign33305195433051954Human1name
152090244CV1581763single nucleotide variantNM_000404.4(GLB1):c.411T>C (p.Ala137=)Mucopolysaccharidosis, MPS-IV-B [RCV002077608]likely benign33306827633068276Human1name
152028568CV1587028single nucleotide variantNM_000404.4(GLB1):c.903G>T (p.Ala301=)Mucopolysaccharidosis, MPS-IV-B [RCV002085505]likely benign33305189433051894Human1name
152172220CV1599034single nucleotide variantNM_000404.4(GLB1):c.426A>G (p.Lys142=)Mucopolysaccharidosis, MPS-IV-B [RCV002143704]likely benign33306826133068261Human1name
152042216CV1619581single nucleotide variantNM_000404.4(GLB1):c.945C>T (p.Ala315=)Mucopolysaccharidosis, MPS-IV-B [RCV002188415]likely benign33305176833051768Human1name
152032105CV1629319single nucleotide variantNM_000404.4(GLB1):c.636G>A (p.Gly212=)Mucopolysaccharidosis, MPS-IV-B [RCV002106295]likely benign33305818633058186Human1name
152054475CV1633057single nucleotide variantNM_000404.4(GLB1):c.789C>T (p.Pro263=)Mucopolysaccharidosis, MPS-IV-B [RCV002127606]likely benign33305349433053494Human1name
152108006CV1657420single nucleotide variantNM_000404.4(GLB1):c.597C>T (p.Tyr199=)Mucopolysaccharidosis, MPS-IV-B [RCV002215080]likely benign33305822533058225Human1name
156030673CV1910731single nucleotide variantNM_000404.4(GLB1):c.67G>A (p.Gly23Ser)Mucopolysaccharidosis, MPS-IV-B [RCV002619839]uncertain significance33309701933097019Human1name
10048105CV192235deletionNM_000404.4(GLB1):c.169del (p.Tyr57fs)not provided [RCV000175596]pathogenic33307262033072620Humanname
156415974CV1966370single nucleotide variantNM_000404.4(GLB1):c.666A>G (p.Gly222=)Mucopolysaccharidosis, MPS-IV-B [RCV002589459]likely benign33305815633058156Human1name
156348042CV1970660single nucleotide variantNM_000404.4(GLB1):c.990C>T (p.Ser330=)Mucopolysaccharidosis, MPS-IV-B [RCV002601627]likely benign33304619833046198Human1name
156241396CV1973224single nucleotide variantNM_000404.4(GLB1):c.699G>T (p.Leu233=)Mucopolysaccharidosis, MPS-IV-B [RCV002597158]likely benign33305812333058123Human1name
156381898CV1978892single nucleotide variantNM_000404.4(GLB1):c.429G>A (p.Glu143=)Mucopolysaccharidosis, MPS-IV-B [RCV002604025]likely benign33306825833068258Human1name
156256566CV2003910single nucleotide variantNM_000404.4(GLB1):c.693G>A (p.Gly231=)Mucopolysaccharidosis, MPS-IV-B [RCV002627625]likely benign33305812933058129Human1name
156198988CV2024466single nucleotide variantNM_000404.4(GLB1):c.462C>T (p.Tyr154=)Mucopolysaccharidosis, MPS-IV-B [RCV002711335]likely benign33306555333065553Human1name
155966953CV2034343single nucleotide variantNM_000404.4(GLB1):c.678A>T (p.Thr226=)Mucopolysaccharidosis, MPS-IV-B [RCV002731438]likely benign33305814433058144Human1name
156341975CV2055448single nucleotide variantNM_000404.4(GLB1):c.729A>G (p.Gly243=)Mucopolysaccharidosis, MPS-IV-B [RCV002811249]likely benign33305809333058093Human1name
156308590CV2067105single nucleotide variantNM_000404.4(GLB1):c.558A>G (p.Glu186=)Mucopolysaccharidosis, MPS-IV-B [RCV002833986]likely benign33305826433058264Human1name
155982812CV2070202single nucleotide variantNM_000404.4(GLB1):c.639T>C (p.Asp213=)Mucopolysaccharidosis, MPS-IV-B [RCV002842604]likely benign33305818333058183Human1name
155979353CV2081893single nucleotide variantNM_000404.4(GLB1):c.879C>G (p.Leu293=)Mucopolysaccharidosis, MPS-IV-B [RCV002863692]likely benign33305191833051918Human1name
156318404CV2090476single nucleotide variantNM_000404.4(GLB1):c.492C>G (p.Val164=)Mucopolysaccharidosis, MPS-IV-B [RCV002899133]likely benign33306552333065523Human1name
156031621CV2093550single nucleotide variantNM_000404.4(GLB1):c.510G>A (p.Lys170=)Mucopolysaccharidosis, MPS-IV-B [RCV002885424]likely benign33306550533065505Human1name
156052136CV2093553single nucleotide variantNM_000404.4(GLB1):c.621T>C (p.Phe207=)Mucopolysaccharidosis, MPS-IV-B [RCV002867818]likely benign33305820133058201Human1name
156043956CV2094261single nucleotide variantNM_000404.4(GLB1):c.62C>T (p.Thr21Met)Inborn genetic diseases [RCV004973678]|Mucopolysaccharidosis, MPS-IV-B [RCV002885921]uncertain significance33309702433097024Human2name
156331627CV2094847single nucleotide variantNM_000404.4(GLB1):c.399A>G (p.Gly133=)Mucopolysaccharidosis, MPS-IV-B [RCV002899958]uncertain significance33306828833068288Human1name
155990981CV2095469single nucleotide variantNM_000404.4(GLB1):c.804A>G (p.Glu268=)Mucopolysaccharidosis, MPS-IV-B [RCV002908158]likely benign33305199333051993Human1name
156351530CV2122414single nucleotide variantNM_000404.4(GLB1):c.87G>T (p.Gln29His)Mucopolysaccharidosis, MPS-IV-B [RCV002966334]uncertain significance33307270233072702Human1name
155954563CV2143872single nucleotide variantNM_000404.4(GLB1):c.68G>A (p.Gly23Asp)Mucopolysaccharidosis, MPS-IV-B [RCV002994820]|not provided [RCV005425019]uncertain significance33309701833097018Human1name
155992197CV2147653single nucleotide variantNM_000404.4(GLB1):c.768G>A (p.Arg256=)Mucopolysaccharidosis, MPS-IV-B [RCV003016880]likely benign33305351533053515Human1name
156027704CV2156173single nucleotide variantNM_000404.4(GLB1):c.363G>A (p.Arg121=)Mucopolysaccharidosis, MPS-IV-B [RCV003018537]likely benign33306885333068853Human1name
156355161CV2188703single nucleotide variantNM_000404.4(GLB1):c.627C>T (p.His209=)Mucopolysaccharidosis, MPS-IV-B [RCV003048632]likely benign33305819533058195Human1name
11551446CV251094single nucleotide variantNM_000404.4(GLB1):c.858C>T (p.Thr286=)GM1 gangliosidosis type 2 [RCV000667352]|Mucopolysaccharidosis, MPS-IV-B [RCV000926956]|not provided [RCV004567802]|not specified [RCV000253060]likely benign33305193933051939Human2name , alternate_id
11544549CV251095single nucleotide variantNM_000404.4(GLB1):c.756C>T (p.Phe252=)GM1 gangliosidosis [RCV001145883]|Mucopolysaccharidosis, MPS-IV-B [RCV000873684]|Mucopolysaccharidosis, MPS-IV-B [RCV001145884]|not provided [RCV001540245]|not specified [RCV000243941]benign|likely benign33305352733053527Human2name
404988174CV3083991single nucleotide variantNM_000404.4(GLB1):c.936C>G (p.Thr312=)Mucopolysaccharidosis, MPS-IV-B [RCV003782183]likely benign33305177733051777Human1name
402513319CV3089431deletionNM_000404.4(GLB1):c.1143+20_1143+21delMucopolysaccharidosis, MPS-IV-B [RCV003780464]likely benign33302423033024231Human1name
402491683CV3091099single nucleotide variantNM_000404.4(GLB1):c.384A>G (p.Ala128=)Mucopolysaccharidosis, MPS-IV-B [RCV003787604]likely benign33306883233068832Human1name
404992613CV3091425single nucleotide variantNM_000404.4(GLB1):c.349C>T (p.Leu117=)Mucopolysaccharidosis, MPS-IV-B [RCV003792900]likely benign33306886733068867Human1name
402497080CV3092558single nucleotide variantNM_000404.4(GLB1):c.435T>C (p.Ile145=)Mucopolysaccharidosis, MPS-IV-B [RCV003788178]likely benign33306825233068252Human1name
402497791CV3092787single nucleotide variantNM_000404.4(GLB1):c.576C>T (p.Tyr192=)Mucopolysaccharidosis, MPS-IV-B [RCV003788251]likely benign33305824633058246Human1name
402486057CV3093854single nucleotide variantNM_000404.4(GLB1):c.606C>T (p.Phe202=)Mucopolysaccharidosis, MPS-IV-B [RCV003787055]likely benign33305821633058216Human1name
405054104CV3094956single nucleotide variantNM_000404.4(GLB1):c.327G>C (p.Arg109=)Mucopolysaccharidosis, MPS-IV-B [RCV003798270]likely benign33306888933068889Human1name
405005277CV3096008single nucleotide variantNM_000404.4(GLB1):c.981G>A (p.Gln327=)Mucopolysaccharidosis, MPS-IV-B [RCV003794158]likely benign33304620733046207Human1name
405010335CV3096555single nucleotide variantNM_000404.4(GLB1):c.936C>A (p.Thr312=)Mucopolysaccharidosis, MPS-IV-B [RCV003794544]likely benign33305177733051777Human1name
404999353CV3099151single nucleotide variantNM_000404.4(GLB1):c.633G>A (p.Leu211=)Mucopolysaccharidosis, MPS-IV-B [RCV003793572]likely benign33305818933058189Human1name
405016904CV3100699single nucleotide variantNM_000404.4(GLB1):c.747A>T (p.Thr249=)Mucopolysaccharidosis, MPS-IV-B [RCV003805447]likely benign33305353633053536Human1name
405021043CV3101263single nucleotide variantNM_000404.4(GLB1):c.321T>C (p.Phe107=)Mucopolysaccharidosis, MPS-IV-B [RCV003805842]likely benign33306889533068895Human1name
405021236CV3101282single nucleotide variantNM_000404.4(GLB1):c.516C>T (p.Leu172=)Mucopolysaccharidosis, MPS-IV-B [RCV003805861]likely benign33306549933065499Human1name
405021247CV3101283single nucleotide variantNM_000404.4(GLB1):c.447C>T (p.Ser149=)Mucopolysaccharidosis, MPS-IV-B [RCV003805862]likely benign33306824033068240Human1name
405180779CV3101771single nucleotide variantNM_000404.4(GLB1):c.696C>T (p.Ala232=)Mucopolysaccharidosis, MPS-IV-B [RCV003803985]likely benign33305812633058126Human1name
405003382CV3102164single nucleotide variantNM_000404.4(GLB1):c.378C>T (p.Ile126=)Mucopolysaccharidosis, MPS-IV-B [RCV003804210]likely benign33306883833068838Human1name
405168947CV3104162single nucleotide variantNM_000404.4(GLB1):c.780C>T (p.Pro260=)Mucopolysaccharidosis, MPS-IV-B [RCV003802839]likely benign33305350333053503Human1name
405172256CV3104635single nucleotide variantNM_000404.4(GLB1):c.771G>A (p.Lys257=)Mucopolysaccharidosis, MPS-IV-B [RCV003803133]likely benign33305351233053512Human1name
405174329CV3104871single nucleotide variantNM_000404.4(GLB1):c.786A>C (p.Gly262=)Mucopolysaccharidosis, MPS-IV-B [RCV003803369]likely benign33305349733053497Human1name
405079889CV3107278single nucleotide variantNM_000404.4(GLB1):c.882T>C (p.Tyr294=)Mucopolysaccharidosis, MPS-IV-B [RCV003800148]likely benign33305191533051915Human1name
405081189CV3107379single nucleotide variantNM_000404.4(GLB1):c.750T>C (p.Asp250=)Mucopolysaccharidosis, MPS-IV-B [RCV003800249]likely benign33305353333053533Human1name
405058350CV3108237single nucleotide variantNM_000404.4(GLB1):c.318T>C (p.Tyr106=)Mucopolysaccharidosis, MPS-IV-B [RCV003808815]likely benign33306889833068898Human1name
405108983CV3112448single nucleotide variantNM_000404.4(GLB1):c.579T>C (p.Phe193=)Mucopolysaccharidosis, MPS-IV-B [RCV003813291]likely benign33305824333058243Human1name
405104924CV3113141single nucleotide variantNM_000404.4(GLB1):c.631C>T (p.Leu211=)Mucopolysaccharidosis, MPS-IV-B [RCV003812432]likely benign33305819133058191Human1name
405106244CV3113390single nucleotide variantNM_000404.4(GLB1):c.504G>A (p.Lys168=)Mucopolysaccharidosis, MPS-IV-B [RCV003812682]likely benign33306551133065511Human1name
405691419CV3227535microsatelliteNM_000404.4(GLB1):c.76-4399_76-4397delInfantile GM1 gangliosidosis [RCV003991880]uncertain significance33307711033077112Humanname , alternate_id
597857860CV3864722single nucleotide variantNM_000404.4(GLB1):c.447C>G (p.Ser149=)Mucopolysaccharidosis, MPS-IV-B [RCV005213778]likely benign33306824033068240Human1name
597850389CV3873267single nucleotide variantNM_000404.4(GLB1):c.375C>T (p.Tyr125=)Mucopolysaccharidosis, MPS-IV-B [RCV005212709]likely benign33306884133068841Human1name
597843327CV3878447single nucleotide variantNM_000404.4(GLB1):c.825T>C (p.Asp275=)Mucopolysaccharidosis, MPS-IV-B [RCV005226937]likely benign33305197233051972Human1name
597928259CV3878880single nucleotide variantNM_000404.4(GLB1):c.77A>G (p.Asn26Ser)Mucopolysaccharidosis, MPS-IV-B [RCV005224539]uncertain significance33307271233072712Human1name
12906004CV413623single nucleotide variantNM_000404.4(GLB1):c.31C>G (p.Leu11Val)GLB1-related disorder [RCV004541535]|Infantile GM1 gangliosidosis [RCV001335294]|Mucopolysaccharidosis, MPS-IV-B [RCV001089162]|not provided [RCV000488298]|not specified [RCV005407147]likely benign|conflicting interpretations of pathogenicity|uncertain significance33309705533097055Human3name , alternate_id
13786056CV543195single nucleotide variantNM_000404.4(GLB1):c.501C>T (p.Pro167=)GM1 gangliosidosis type 2 [RCV000672524]uncertain significance33306551433065514Human1name , alternate_id
13789968CV543208single nucleotide variantNM_000404.4(GLB1):c.93G>A (p.Met31Ile)GM1 gangliosidosis type 2 [RCV000666272]uncertain significance33307269633072696Human1name , alternate_id
14710083CV631178deletionNM_000404.4(GLB1):c.163del (p.Ile55fs)Mucopolysaccharidosis, MPS-IV-B [RCV000813662]pathogenic33307262633072626Human1name
15122905CV691377single nucleotide variantNM_000404.4(GLB1):c.327G>A (p.Arg109=)Mucopolysaccharidosis, MPS-IV-B [RCV000874495]likely benign33306888933068889Human1name
15170592CV708788single nucleotide variantNM_000404.4(GLB1):c.534G>A (p.Gly178=)GM1 gangliosidosis [RCV001148906]|Inborn genetic diseases [RCV004973213]|Mucopolysaccharidosis, MPS-IV-B [RCV000972042]|Mucopolysaccharidosis, MPS-IV-B [RCV001148907]likely benign|uncertain significance33306548133065481Human3name
15149414CV734029single nucleotide variantNM_000404.4(GLB1):c.693G>C (p.Gly231=)Mucopolysaccharidosis, MPS-IV-B [RCV000900929]likely benign33305812933058129Human1name
15101853CV748207single nucleotide variantNM_000404.4(GLB1):c.909G>A (p.Val303=)Mucopolysaccharidosis, MPS-IV-B [RCV002065866]likely benign33305188833051888Human1name
15147568CV763819single nucleotide variantNM_000404.4(GLB1):c.849A>C (p.Thr283=)Mucopolysaccharidosis, MPS-IV-B [RCV001488482]likely benign33305194833051948Human1name
15177332CV763820single nucleotide variantNM_000404.4(GLB1):c.780C>G (p.Pro260=)Mucopolysaccharidosis, MPS-IV-B [RCV000929129]|not provided [RCV003432927]likely benign33305350333053503Human1name
15192507CV763821single nucleotide variantNM_000404.4(GLB1):c.777G>A (p.Glu259=)Mucopolysaccharidosis, MPS-IV-B [RCV002066119]likely benign33305350633053506Human1name
8624263CV79372single nucleotide variantNM_000404.4(GLB1):c.456A>T (p.Pro152=)GM1 gangliosidosis type 2 [RCV000059353]not provided33306823133068231Humanname
28871508CV888671single nucleotide variantNM_000404.4(GLB1):c.711C>T (p.Tyr237=)GM1 gangliosidosis [RCV001145885]|Mucopolysaccharidosis, MPS-IV-B [RCV001145886]|Mucopolysaccharidosis, MPS-IV-B [RCV001406952]likely benign|uncertain significance33305811133058111Human2name
8639828CV98811single nucleotide variantNM_000404.4(GLB1):c.29C>T (p.Pro10Leu)GM1 gangliosidosis [RCV000340960]|GM1 gangliosidosis type 2 [RCV001701735]|GM1 gangliosidosis type 3 [RCV001701656]|Infantile GM1 gangliosidosis [RCV001527573]|Mucopolysaccharidosis, MPS-IV-B [RCV000402607]|Mucopolysaccharidosis, MPS-IV-B [RCV001511462]|not provided [RCV000590040]|not specified [RCVbenign|conflicting interpretations of pathogenicity|conflicting data from submitters33309705733097057Human5name , alternate_id
126725103CV1016237single nucleotide variantNM_000404.4(GLB1):c.235G>A (p.Ala79Thr)GM1 gangliosidosis type 3 [RCV001331202]|Mucopolysaccharidosis, MPS-IV-B [RCV002546453]|not provided [RCV004692544]uncertain significance33307255433072554Human2name
126909283CV1042151single nucleotide variantNM_000404.4(GLB1):c.107A>G (p.Tyr36Cys)GM1 gangliosidosis type 2 [RCV005023114]|Mucopolysaccharidosis, MPS-IV-B [RCV001373808]|Mucopolysaccharidosis, MPS-IV-B [RCV005236841]|not provided [RCV004728689]pathogenic|likely pathogenic|uncertain significance33307268233072682Human2name , alternate_id
127257042CV1055333single nucleotide variantNM_000404.4(GLB1):c.202C>G (p.Arg68Gly)Mucopolysaccharidosis, MPS-IV-B [RCV001379676]likely pathogenic33307258733072587Human1name
127264745CV1059734deletionNM_000404.4(GLB1):c.473del (p.Val158fs)Mucopolysaccharidosis, MPS-IV-B [RCV001381302]pathogenic33306554233065542Human1name
127237814CV1070678single nucleotide variantNM_000404.4(GLB1):c.2031A>G (p.Val677=)Mucopolysaccharidosis, MPS-IV-B [RCV001392377]likely benign33299704832997048Human1name
127249465CV1070679single nucleotide variantNM_000404.4(GLB1):c.1983C>T (p.Leu661=)Mucopolysaccharidosis, MPS-IV-B [RCV001417326]|not provided [RCV002264306]likely benign33299709632997096Human1name
127282207CV1070680single nucleotide variantNM_000404.4(GLB1):c.1980A>G (p.Arg660=)Mucopolysaccharidosis, MPS-IV-B [RCV001410995]likely benign33299709932997099Human1name
127252949CV1070681single nucleotide variantNM_000404.4(GLB1):c.1833G>C (p.Ser611=)Mucopolysaccharidosis, MPS-IV-B [RCV001400441]likely benign33299724632997246Human1name
127233577CV1070682single nucleotide variantNM_000404.4(GLB1):c.1803G>A (p.Leu601=)Mucopolysaccharidosis, MPS-IV-B [RCV001413951]likely benign33299727632997276Human1name
127243238CV1070687single nucleotide variantNM_000404.4(GLB1):c.1536T>C (p.Phe512=)Mucopolysaccharidosis, MPS-IV-B [RCV001416109]|not provided [RCV002264305]likely benign33301425433014254Human1name
127245473CV1070688single nucleotide variantNM_000404.4(GLB1):c.1495C>T (p.Leu499=)Mucopolysaccharidosis, MPS-IV-B [RCV001398726]likely benign33301429533014295Human1name
127244269CV1070690single nucleotide variantNM_000404.4(GLB1):c.1368G>A (p.Glu456=)Mucopolysaccharidosis, MPS-IV-B [RCV001393686]likely benign33301682033016820Human1name
127278220CV1092370single nucleotide variantNM_000404.4(GLB1):c.1914C>T (p.Phe638=)Mucopolysaccharidosis, MPS-IV-B [RCV001444910]likely benign33299716532997165Human1name
127253425CV1092371single nucleotide variantNM_000404.4(GLB1):c.1911G>A (p.Thr637=)Mucopolysaccharidosis, MPS-IV-B [RCV001426040]likely benign33299716832997168Human1name
127232339CV1092372single nucleotide variantNM_000404.4(GLB1):c.1815G>A (p.Gln605=)Mucopolysaccharidosis, MPS-IV-B [RCV001421274]likely benign33299726432997264Human1name
127276230CV1092373single nucleotide variantNM_000404.4(GLB1):c.1650C>G (p.Ala550=)Mucopolysaccharidosis, MPS-IV-B [RCV001443720]likely benign33301414033014140Human1name
127249069CV1092374single nucleotide variantNM_000404.4(GLB1):c.1593C>T (p.Asp531=)Mucopolysaccharidosis, MPS-IV-B [RCV001425044]likely benign33301419733014197Human1name
127245832CV1092375single nucleotide variantNM_000404.4(GLB1):c.1512T>C (p.Asn504=)Mucopolysaccharidosis, MPS-IV-B [RCV001435282]likely benign33301427833014278Human1name
127284262CV1092377single nucleotide variantNM_000404.4(GLB1):c.1101A>G (p.Pro367=)Mucopolysaccharidosis, MPS-IV-B [RCV001449178]likely benign33302429333024293Human1name
127271614CV1092378single nucleotide variantNM_000404.4(GLB1):c.1020T>C (p.Ala340=)Mucopolysaccharidosis, MPS-IV-B [RCV001431029]likely benign33304616833046168Human1name
127331100CV1113893single nucleotide variantNM_000404.4(GLB1):c.2028T>C (p.His676=)Mucopolysaccharidosis, MPS-IV-B [RCV001471327]likely benign33299705132997051Human1name
127294874CV1113894single nucleotide variantNM_000404.4(GLB1):c.2007C>T (p.Asn669=)Mucopolysaccharidosis, MPS-IV-B [RCV001459577]likely benign33299707232997072Human1name
127331622CV1113895single nucleotide variantNM_000404.4(GLB1):c.1989C>T (p.Pro663=)Mucopolysaccharidosis, MPS-IV-B [RCV001471696]likely benign33299709032997090Human1name
127297344CV1113896single nucleotide variantNM_000404.4(GLB1):c.1896A>G (p.Glu632=)Mucopolysaccharidosis, MPS-IV-B [RCV001453034]likely benign33299718332997183Human1name
127299431CV1113898single nucleotide variantNM_000404.4(GLB1):c.1521G>A (p.Thr507=)Mucopolysaccharidosis, MPS-IV-B [RCV001460807]|not provided [RCV004711651]likely benign33301426933014269Human1name
127301740CV1113901single nucleotide variantNM_000404.4(GLB1):c.1449G>T (p.Val483=)Mucopolysaccharidosis, MPS-IV-B [RCV001461469]likely benign33301673933016739Human1name
127330767CV1113903single nucleotide variantNM_000404.4(GLB1):c.1257G>A (p.Arg419=)Mucopolysaccharidosis, MPS-IV-B [RCV001471120]likely benign33301853833018538Human1name
127336216CV1113904single nucleotide variantNM_000404.4(GLB1):c.1215A>C (p.Thr405=)Mucopolysaccharidosis, MPS-IV-B [RCV001474827]likely benign33302158433021584Human1name
127326967CV1113905single nucleotide variantNM_000404.4(GLB1):c.1074A>G (p.Glu358=)Mucopolysaccharidosis, MPS-IV-B [RCV001468943]|not provided [RCV003438816]likely benign33302432033024320Human1name
127335098CV1113906single nucleotide variantNM_000404.4(GLB1):c.1008A>G (p.Pro336=)Mucopolysaccharidosis, MPS-IV-B [RCV001474014]likely benign33304618033046180Human1name
127327696CV1134781single nucleotide variantNM_000404.4(GLB1):c.1995C>T (p.Pro665=)Mucopolysaccharidosis, MPS-IV-B [RCV001506768]likely benign33299708432997084Human1name
127307582CV1134782single nucleotide variantNM_000404.4(GLB1):c.1950C>T (p.Tyr650=)Mucopolysaccharidosis, MPS-IV-B [RCV001500527]likely benign33299712932997129Human1name
127298833CV1134783single nucleotide variantNM_000404.4(GLB1):c.1851C>T (p.Thr617=)Mucopolysaccharidosis, MPS-IV-B [RCV001498165]likely benign33299722832997228Human1name
127324436CV1134784single nucleotide variantNM_000404.4(GLB1):c.1812C>G (p.Pro604=)Mucopolysaccharidosis, MPS-IV-B [RCV001485480]likely benign33299726732997267Human1name
127315134CV1134785single nucleotide variantNM_000404.4(GLB1):c.1620C>T (p.Ala540=)Mucopolysaccharidosis, MPS-IV-B [RCV001482452]likely benign33301417033014170Human1name
127286393CV1134786single nucleotide variantNM_000404.4(GLB1):c.1605T>C (p.His535=)Mucopolysaccharidosis, MPS-IV-B [RCV001494148]likely benign33301418533014185Human1name
127313977CV1134787single nucleotide variantNM_000404.4(GLB1):c.1515C>T (p.Ile505=)Mucopolysaccharidosis, MPS-IV-B [RCV001482116]likely benign33301427533014275Human1name
127290487CV1134788single nucleotide variantNM_000404.4(GLB1):c.1470C>T (p.Asn490=)Mucopolysaccharidosis, MPS-IV-B [RCV001495989]likely benign33301671833016718Human1name
127312102CV1134789single nucleotide variantNM_000404.4(GLB1):c.1293T>C (p.Pro431=)Mucopolysaccharidosis, MPS-IV-B [RCV001481607]likely benign33301850233018502Human1name
127318922CV1134790single nucleotide variantNM_000404.4(GLB1):c.1263A>G (p.Thr421=)Mucopolysaccharidosis, MPS-IV-B [RCV001483657]likely benign33301853233018532Human1name
150555687CV1304842single nucleotide variantNM_000404.4(GLB1):c.271C>A (p.Pro91Thr)not provided [RCV001773090]uncertain significance33306894533068945Humanname
151351353CV1323496single nucleotide variantNM_000404.4(GLB1):c.266A>T (p.His89Leu)Infantile GM1 gangliosidosis [RCV001806352]pathogenic33306895033068950Human1name , alternate_id
151799085CV1344433single nucleotide variantNM_000404.4(GLB1):c.1647G>A (p.Pro549=)Mucopolysaccharidosis, MPS-IV-B [RCV001919098]likely benign|uncertain significance33301414333014143Human1name
151776259CV1374570single nucleotide variantNM_000404.4(GLB1):c.168C>G (p.His56Gln)Mucopolysaccharidosis, MPS-IV-B [RCV001875703]|not specified [RCV002282633]uncertain significance33307262133072621Human1name
151715286CV1376229single nucleotide variantNM_000404.4(GLB1):c.176G>T (p.Arg59Leu)Mucopolysaccharidosis, MPS-IV-B [RCV002019499]likely pathogenic33307261333072613Human1name
151786888CV1417827single nucleotide variantNM_000404.4(GLB1):c.295T>A (p.Ser99Thr)Mucopolysaccharidosis, MPS-IV-B [RCV001894777]uncertain significance33306892133068921Human1name
151709766CV1428637single nucleotide variantNM_000404.4(GLB1):c.1146A>G (p.Leu382=)Mucopolysaccharidosis, MPS-IV-B [RCV001994786]likely benign33302165333021653Human1name
151711501CV1442007single nucleotide variantNM_000404.4(GLB1):c.203G>T (p.Arg68Leu)Mucopolysaccharidosis, MPS-IV-B [RCV002002980]|not specified [RCV003323967]likely pathogenic|uncertain significance33307258633072586Human1name
151809428CV1454280single nucleotide variantNM_000404.4(GLB1):c.173C>T (p.Ser58Phe)Mucopolysaccharidosis, MPS-IV-B [RCV001938792]uncertain significance33307261633072616Human1name
151718289CV1485489single nucleotide variantNM_000404.4(GLB1):c.161G>A (p.Ser54Asn)GM1 gangliosidosis [RCV005238174]|Mucopolysaccharidosis, MPS-IV-B [RCV002029304]likely pathogenic33307262833072628Human2name
151770595CV1512805single nucleotide variantNM_000404.4(GLB1):c.257G>A (p.Trp86Ter)Mucopolysaccharidosis, MPS-IV-B [RCV001866791]pathogenic33306895933068959Human1name
152082351CV1526174single nucleotide variantNM_000404.4(GLB1):c.1764T>C (p.Leu588=)Mucopolysaccharidosis, MPS-IV-B [RCV002170702]likely benign33299731532997315Human1name
152108589CV1529995single nucleotide variantNM_000404.4(GLB1):c.1017G>A (p.Glu339=)Mucopolysaccharidosis, MPS-IV-B [RCV002196476]likely benign33304617133046171Human1name
152136762CV1537843single nucleotide variantNM_000404.4(GLB1):c.1794G>A (p.Gln598=)Mucopolysaccharidosis, MPS-IV-B [RCV002177523]likely benign33299728532997285Human1name
152117397CV1538867single nucleotide variantNM_000404.4(GLB1):c.1935C>A (p.Gly645=)Mucopolysaccharidosis, MPS-IV-B [RCV002175115]likely benign33299714432997144Human1name
152045552CV1556141single nucleotide variantNM_000404.4(GLB1):c.1062C>T (p.Ile354=)Mucopolysaccharidosis, MPS-IV-B [RCV002206883]likely benign33304612633046126Human1name
152165873CV1557112single nucleotide variantNM_000404.4(GLB1):c.1566C>T (p.Ser522=)Mucopolysaccharidosis, MPS-IV-B [RCV002181825]likely benign33301422433014224Human1name
152046189CV1561391single nucleotide variantNM_000404.4(GLB1):c.1320C>T (p.His440=)Mucopolysaccharidosis, MPS-IV-B [RCV002108366]likely benign33301847533018475Human1name
152051448CV1569278single nucleotide variantNM_000404.4(GLB1):c.1704C>T (p.Asp568=)Mucopolysaccharidosis, MPS-IV-B [RCV002207572]likely benign33301408633014086Human1name
152145166CV1582626single nucleotide variantNM_000404.4(GLB1):c.1638C>T (p.Tyr546=)Mucopolysaccharidosis, MPS-IV-B [RCV002201127]likely benign33301415233014152Human1name
152149149CV1593104single nucleotide variantNM_000404.4(GLB1):c.1377T>C (p.Asn459=)Mucopolysaccharidosis, MPS-IV-B [RCV002101953]likely benign33301681133016811Human1name
152093478CV1593472single nucleotide variantNM_000404.4(GLB1):c.1176G>A (p.Leu392=)Mucopolysaccharidosis, MPS-IV-B [RCV002094515]likely benign33302162333021623Human1name
8595215CV15962single nucleotide variantNM_000404.4(GLB1):c.145C>T (p.Arg49Cys)GM1 gangliosidosis type 2 [RCV000672371]|Infantile GM1 gangliosidosis [RCV000000971]|Mucopolysaccharidosis, MPS-IV-B [RCV000707313]|Mucopolysaccharidosis, MPS-IV-B [RCV001778644]|not provided [RCV000175599]pathogenic|likely pathogenic|uncertain significance|no classifications from unflagged records33307264433072644Human3name , alternate_id
8595218CV15965single nucleotide variantNM_000404.4(GLB1):c.152T>C (p.Ile51Thr)GM1 gangliosidosis type 2 [RCV000671053]|GM1 gangliosidosis type 3 [RCV000000974]|Infantile GM1 gangliosidosis [RCV001582457]|Mucopolysaccharidosis, MPS-IV-B [RCV001851520]|Mucopolysaccharidosis, MPS-IV-B [RCV004799723]pathogenic|not provided33307263733072637Human4name , alternate_id
8595225CV15974single nucleotide variantNM_000404.4(GLB1):c.245C>T (p.Thr82Met)GM1 gangliosidosis type 2 [RCV000669063]|GM1 gangliosidosis type 3 [RCV000000984]|Inborn genetic diseases [RCV000624609]|Infantile GM1 gangliosidosis [RCV004546408]|Mucopolysaccharidosis, MPS-IV-B [RCV001068811]|not provided [RCV001559063]pathogenic|likely pathogenic|uncertain significance|no classifications from unflagged records33307254433072544Human5name , alternate_id
8595226CV15976single nucleotide variantNM_000404.4(GLB1):c.247T>C (p.Tyr83His)Mucopolysaccharidosis, MPS-IV-B [RCV000000986]pathogenic33306896933068969Human1name
8595232CV15983single nucleotide variantNM_000404.4(GLB1):c.202C>T (p.Arg68Trp)GM1 gangliosidosis type 2 [RCV000000993]|GM1 gangliosidosis type 2 [RCV005031376]|Infantile GM1 gangliosidosis [RCV000760159]|Mucopolysaccharidosis, MPS-IV-B [RCV001235447]|not provided [RCV004589492]pathogenic|likely pathogenic33307258733072587Human3name , alternate_id
8595233CV15984single nucleotide variantNM_000404.4(GLB1):c.176G>A (p.Arg59His)GLB1-related disorder [RCV004545719]|GM1 gangliosidosis [RCV000778693]|GM1 gangliosidosis type 2 [RCV000059350]|GM1 gangliosidosis type 2 [RCV000850557]|GM1 gangliosidosis type 3 [RCV000984179]|GM1-gangliosidosis, type I, with cardiac involvement [RCV000000994]|pathogenic|likely pathogenic|not provided33307261333072613Human6name , alternate_id
152114699CV1612567single nucleotide variantNM_000404.4(GLB1):c.1752T>C (p.Asn584=)Mucopolysaccharidosis, MPS-IV-B [RCV002174776]likely benign33299732732997327Human1name
152042424CV1618048single nucleotide variantNM_000404.4(GLB1):c.1251G>A (p.Leu417=)Mucopolysaccharidosis, MPS-IV-B [RCV002206522]likely benign33301854433018544Human1name
152043125CV1618159single nucleotide variantNM_000404.4(GLB1):c.1698C>T (p.Pro566=)Mucopolysaccharidosis, MPS-IV-B [RCV002206604]likely benign33301409233014092Human1name
152030542CV1622235single nucleotide variantNM_000404.4(GLB1):c.1785G>A (p.Arg595=)Mucopolysaccharidosis, MPS-IV-B [RCV002186494]likely benign33299729432997294Human1name
152052143CV1622564single nucleotide variantNM_000404.4(GLB1):c.1215A>G (p.Thr405=)Mucopolysaccharidosis, MPS-IV-B [RCV002207654]likely benign33302158433021584Human1name
152104476CV1622639single nucleotide variantNM_000404.4(GLB1):c.1545C>T (p.Asp515=)Mucopolysaccharidosis, MPS-IV-B [RCV002214617]likely benign33301424533014245Human1name
152112440CV1623639single nucleotide variantNM_000404.4(GLB1):c.1995C>G (p.Pro665=)Mucopolysaccharidosis, MPS-IV-B [RCV002134657]likely benign33299708432997084Human1name
152060267CV1628075single nucleotide variantNM_000404.4(GLB1):c.1656T>C (p.Tyr552=)Mucopolysaccharidosis, MPS-IV-B [RCV002190440]likely benign33301413433014134Human1name
152132153CV1633329single nucleotide variantNM_000404.4(GLB1):c.1174C>T (p.Leu392=)Mucopolysaccharidosis, MPS-IV-B [RCV002137062]likely benign33302162533021625Human1name
152090136CV1634119single nucleotide variantNM_000404.4(GLB1):c.1665C>T (p.Asn555=)Mucopolysaccharidosis, MPS-IV-B [RCV002194187]likely benign33301412533014125Human1name
152135304CV1634421single nucleotide variantNM_000404.4(GLB1):c.1701G>A (p.Gln567=)Mucopolysaccharidosis, MPS-IV-B [RCV002218634]likely benign33301408933014089Human1name
152034426CV1634913single nucleotide variantNM_000404.4(GLB1):c.1572G>C (p.Leu524=)Mucopolysaccharidosis, MPS-IV-B [RCV002086969]likely benign33301421833014218Human1name
152034951CV1639622single nucleotide variantNM_000404.4(GLB1):c.1821C>A (p.Ile607=)Mucopolysaccharidosis, MPS-IV-B [RCV002187340]likely benign33299725832997258Human1name
152118212CV1644075single nucleotide variantNM_000404.4(GLB1):c.1086A>G (p.Glu362=)Mucopolysaccharidosis, MPS-IV-B [RCV002135370]likely benign33302430833024308Human1name
152098519CV1650367single nucleotide variantNM_000404.4(GLB1):c.1317C>G (p.Val439=)Mucopolysaccharidosis, MPS-IV-B [RCV002115020]likely benign33301847833018478Human1name
152029584CV1653339single nucleotide variantNM_000404.4(GLB1):c.1518C>G (p.Leu506=)Mucopolysaccharidosis, MPS-IV-B [RCV002085850]likely benign33301427233014272Human1name
152146882CV1655986single nucleotide variantNM_000404.4(GLB1):c.1959C>T (p.Pro653=)Mucopolysaccharidosis, MPS-IV-B [RCV002220188]likely benign33299712032997120Human1name
155709294CV1775730single nucleotide variantNM_000404.4(GLB1):c.262T>C (p.Phe88Leu)Mucopolysaccharidosis, MPS-IV-B [RCV002296121]uncertain significance33306895433068954Human1name
155736133CV1781922deletionNM_000404.4(GLB1):c.835del (p.Gln279fs)GM1 gangliosidosis type 2 [RCV002309663]likely pathogenic33305196233051962Human1name , alternate_id
156407077CV1874805single nucleotide variantNM_000404.4(GLB1):c.1314A>C (p.Gly438=)Mucopolysaccharidosis, MPS-IV-B [RCV003070720]likely benign33301848133018481Human1name
156353459CV1879960single nucleotide variantNM_000404.4(GLB1):c.1917G>C (p.Val639=)Mucopolysaccharidosis, MPS-IV-B [RCV003065045]likely benign33299716232997162Human1name
156276914CV1880694single nucleotide variantNM_000404.4(GLB1):c.1599C>A (p.Gly533=)Mucopolysaccharidosis, MPS-IV-B [RCV003060927]likely benign33301419133014191Human1name
156409529CV1881272single nucleotide variantNM_000404.4(GLB1):c.1641G>T (p.Thr547=)Mucopolysaccharidosis, MPS-IV-B [RCV003071708]likely benign33301414933014149Human1name
156252795CV1883956single nucleotide variantNM_000404.4(GLB1):c.1557A>G (p.Ala519=)Mucopolysaccharidosis, MPS-IV-B [RCV003086164]|not provided [RCV003435871]likely benign33301423333014233Human1name
156017984CV1885418single nucleotide variantNM_000404.4(GLB1):c.1311T>C (p.Asn437=)Mucopolysaccharidosis, MPS-IV-B [RCV003077469]likely benign33301848433018484Human1name
156235095CV1885428single nucleotide variantNM_000404.4(GLB1):c.1899A>G (p.Leu633=)Mucopolysaccharidosis, MPS-IV-B [RCV003085526]likely benign33299718032997180Human1name
156024161CV1895941single nucleotide variantNM_000404.4(GLB1):c.1176G>T (p.Leu392=)Mucopolysaccharidosis, MPS-IV-B [RCV003100346]likely benign33302162333021623Human1name
10049655CV190747single nucleotide variantNM_000404.4(GLB1):c.1068G>A (p.Lys356=)not provided [RCV000173687]uncertain significance33304612033046120Humanname
156032349CV1910903single nucleotide variantNM_000404.4(GLB1):c.1905T>C (p.Ala635=)Mucopolysaccharidosis, MPS-IV-B [RCV002619907]likely benign33299717432997174Human1name
10048106CV192236single nucleotide variantNM_000404.4(GLB1):c.203G>A (p.Arg68Gln)GM1 gangliosidosis [RCV001201192]|GM1 gangliosidosis type 2 [RCV000673880]|Mucopolysaccharidosis, MPS-IV-B [RCV001852152]|not provided [RCV000175606]pathogenic|likely pathogenic|uncertain significance|no classifications from unflagged records33307258633072586Human3name , alternate_id
156445200CV1945200single nucleotide variantNM_000404.4(GLB1):c.119C>T (p.Ser40Phe)Mucopolysaccharidosis, MPS-IV-B [RCV003116140]uncertain significance33307267033072670Human1name
156446987CV1948681single nucleotide variantNM_000404.4(GLB1):c.1653T>C (p.Phe551=)Mucopolysaccharidosis, MPS-IV-B [RCV003118511]likely benign33301413733014137Human1name
156446062CV1951088single nucleotide variantNM_000404.4(GLB1):c.1725A>T (p.Gly575=)Mucopolysaccharidosis, MPS-IV-B [RCV003117025]likely benign33301406533014065Human1name
156236735CV1973021deletionNM_000404.4(GLB1):c.485del (p.Leu162fs)Mucopolysaccharidosis, MPS-IV-B [RCV002597004]pathogenic33306553033065530Human1name
156394381CV1983611single nucleotide variantNM_000404.4(GLB1):c.189C>G (p.Phe63Leu)Mucopolysaccharidosis, MPS-IV-B [RCV002604990]uncertain significance33307260033072600Human1name
156401412CV2013403single nucleotide variantNM_000404.4(GLB1):c.1725A>G (p.Gly575=)Mucopolysaccharidosis, MPS-IV-B [RCV002726037]likely benign33301406533014065Human1name
156201769CV2021255single nucleotide variantNM_000404.4(GLB1):c.1176G>C (p.Leu392=)Mucopolysaccharidosis, MPS-IV-B [RCV002711425]likely benign33302162333021623Human1name
155984435CV2030322single nucleotide variantNM_000404.4(GLB1):c.1338T>C (p.Ala446=)Mucopolysaccharidosis, MPS-IV-B [RCV002755473]likely benign33301845733018457Human1name
156008482CV2046346single nucleotide variantNM_000404.4(GLB1):c.1254C>T (p.Tyr418=)Mucopolysaccharidosis, MPS-IV-B [RCV002756549]likely benign33301854133018541Human1name
156019404CV2061833single nucleotide variantNM_000404.4(GLB1):c.1602C>T (p.His534=)Mucopolysaccharidosis, MPS-IV-B [RCV002820540]likely benign33301418833014188Human1name
156059283CV2069153deletionNM_000404.4(GLB1):c.677del (p.Thr226fs)Mucopolysaccharidosis, MPS-IV-B [RCV002846713]pathogenic33305814533058145Human1name
156084310CV2079973single nucleotide variantNM_000404.4(GLB1):c.1854G>C (p.Val618=)Mucopolysaccharidosis, MPS-IV-B [RCV002847491]likely benign33299722532997225Human1name
156226737CV2081139single nucleotide variantNM_000404.4(GLB1):c.1011G>C (p.Leu337=)Mucopolysaccharidosis, MPS-IV-B [RCV002853417]likely benign33304617733046177Human1name
156230339CV2085222deletionNM_000404.4(GLB1):c.344del (p.Gly115fs)Mucopolysaccharidosis, MPS-IV-B [RCV002876213]pathogenic33306887233068872Human1name
156190807CV2086743single nucleotide variantNM_000404.4(GLB1):c.1854G>A (p.Val618=)Mucopolysaccharidosis, MPS-IV-B [RCV002852132]likely benign33299722532997225Human1name
156112657CV2093019single nucleotide variantNM_000404.4(GLB1):c.1716G>A (p.Gln572=)Mucopolysaccharidosis, MPS-IV-B [RCV002913844]likely benign33301407433014074Human1name
156157386CV2094952single nucleotide variantNM_000404.4(GLB1):c.184C>T (p.Arg62Cys)GM1 gangliosidosis type 2 [RCV005400541]|Mucopolysaccharidosis, MPS-IV-B [RCV002890858]uncertain significance33307260533072605Human2name , alternate_id
156325582CV2098254single nucleotide variantNM_000404.4(GLB1):c.1416T>A (p.Thr472=)Mucopolysaccharidosis, MPS-IV-B [RCV002899608]likely benign33301677233016772Human1name
156101036CV2099269deletionNM_000404.4(GLB1):c.833del (p.Gly278fs)GM1 gangliosidosis type 2 [RCV005028010]|Mucopolysaccharidosis, MPS-IV-B [RCV002913404]pathogenic33305196433051964Human2name , alternate_id
155983720CV2101204single nucleotide variantNM_000404.4(GLB1):c.1110A>C (p.Pro370=)Mucopolysaccharidosis, MPS-IV-B [RCV002882056]likely benign33302428433024284Human1name
156113718CV2104518single nucleotide variantNM_000404.4(GLB1):c.1947C>T (p.Thr649=)Mucopolysaccharidosis, MPS-IV-B [RCV002927537]likely benign33299713232997132Human1name
156311770CV2120059single nucleotide variantNM_000404.4(GLB1):c.113G>A (p.Arg38Gln)Mucopolysaccharidosis, MPS-IV-B [RCV002962662]uncertain significance33307267633072676Human1name
156377412CV2124291single nucleotide variantNM_000404.4(GLB1):c.1047T>A (p.Ala349=)Mucopolysaccharidosis, MPS-IV-B [RCV002942852]likely benign33304614133046141Human1name
156013505CV2133800single nucleotide variantNM_000404.4(GLB1):c.1467C>A (p.Ile489=)Mucopolysaccharidosis, MPS-IV-B [RCV003017869]likely benign33301672133016721Human1name
156285029CV2134074single nucleotide variantNM_000404.4(GLB1):c.1647G>C (p.Pro549=)Mucopolysaccharidosis, MPS-IV-B [RCV003009736]likely benign33301414333014143Human1name
155938846CV2146486single nucleotide variantNM_000404.4(GLB1):c.1992A>C (p.Pro664=)Mucopolysaccharidosis, MPS-IV-B [RCV003014130]likely benign33299708732997087Human1name
156323207CV2162976single nucleotide variantNM_000404.4(GLB1):c.268G>C (p.Glu90Gln)Mucopolysaccharidosis, MPS-IV-B [RCV003029314]uncertain significance33306894833068948Human1name
155984025CV2163313single nucleotide variantNM_000404.4(GLB1):c.1680T>C (p.Ser560=)Mucopolysaccharidosis, MPS-IV-B [RCV003034013]likely benign33301411033014110Human1name
156004818CV2166711single nucleotide variantNM_000404.4(GLB1):c.1662G>T (p.Gly554=)Mucopolysaccharidosis, MPS-IV-B [RCV003017442]likely benign33301412833014128Human1name
156000646CV2168085single nucleotide variantNM_000404.4(GLB1):c.1389G>T (p.Leu463=)Mucopolysaccharidosis, MPS-IV-B [RCV003034757]likely benign33301679933016799Human1name
156212654CV2176364single nucleotide variantNM_000404.4(GLB1):c.1635C>T (p.Asn545=)Mucopolysaccharidosis, MPS-IV-B [RCV003024866]likely benign33301415533014155Human1name
155964933CV2179972single nucleotide variantNM_000404.4(GLB1):c.278C>A (p.Pro93Gln)Mucopolysaccharidosis, MPS-IV-B [RCV003033120]uncertain significance33306893833068938Human1name
156350837CV2189650single nucleotide variantNM_000404.4(GLB1):c.209T>C (p.Leu70Pro)Mucopolysaccharidosis, MPS-IV-B [RCV003048321]uncertain significance33307258033072580Human1name
243059832CV2412648single nucleotide variantNM_000404.4(GLB1):c.206T>C (p.Leu69Pro)not provided [RCV003135376]uncertain significance33307258333072583Humanname
13783958CV244010single nucleotide variantNM_000404.4(GLB1):c.276G>A (p.Trp92Ter)GM1 gangliosidosis type 2 [RCV000670448]|Infantile GM1 gangliosidosis [RCV000766231]|Mucopolysaccharidosis, MPS-IV-B [RCV001387511]|not provided [RCV001091797]pathogenic33306894033068940Human3name , alternate_id
329848933CV2523684single nucleotide variantNM_000404.4(GLB1):c.130G>T (p.Asp44Tyr)Infantile GM1 gangliosidosis [RCV003225699]likely pathogenic33307265933072659Human1name , alternate_id
401915181CV2795177single nucleotide variantNM_000404.4(GLB1):c.253C>T (p.Pro85Ser)Mucopolysaccharidosis, MPS-IV-B [RCV003388961]likely pathogenic33306896333068963Human1name
11590140CV290776single nucleotide variantNM_000404.4(GLB1):c.1530G>A (p.Thr510=)GM1 gangliosidosis [RCV000361475]|Mucopolysaccharidosis, MPS-IV-B [RCV000316174]|Mucopolysaccharidosis, MPS-IV-B [RCV000874904]likely benign|uncertain significance33301426033014260Human2name
11588538CV294409single nucleotide variantNM_000404.4(GLB1):c.1032T>C (p.Thr344=)GM1 gangliosidosis [RCV000403633]|Mucopolysaccharidosis, MPS-IV-B [RCV000303902]|Mucopolysaccharidosis, MPS-IV-B [RCV000876887]|not provided [RCV003333979]benign|likely benign|uncertain significance33304615633046156Human2name
404988955CV3084042single nucleotide variantNM_000404.4(GLB1):c.160A>G (p.Ser54Gly)Mucopolysaccharidosis, MPS-IV-B [RCV003782234]likely pathogenic33307262933072629Human1name
404996243CV3085470single nucleotide variantNM_000404.4(GLB1):c.1899A>T (p.Leu633=)Mucopolysaccharidosis, MPS-IV-B [RCV003783001]likely benign33299718032997180Human1name
404997987CV3085768single nucleotide variantNM_000404.4(GLB1):c.2022G>A (p.Leu674=)Mucopolysaccharidosis, MPS-IV-B [RCV003783138]likely benign33299705732997057Human1name
404996552CV3088525single nucleotide variantNM_000404.4(GLB1):c.1455T>C (p.Tyr485=)Mucopolysaccharidosis, MPS-IV-B [RCV003793302]likely benign33301673333016733Human1name
404996688CV3088537single nucleotide variantNM_000404.4(GLB1):c.1380G>A (p.Val460=)Mucopolysaccharidosis, MPS-IV-B [RCV003793314]likely benign33301680833016808Human1name
402490502CV3090983single nucleotide variantNM_000404.4(GLB1):c.1707C>T (p.Thr569=)Mucopolysaccharidosis, MPS-IV-B [RCV003787485]likely benign33301408333014083Human1name
402521081CV3091984single nucleotide variantNM_000404.4(GLB1):c.1119A>T (p.Ala373=)Mucopolysaccharidosis, MPS-IV-B [RCV003790430]likely benign33302427533024275Human1name
402496508CV3092502single nucleotide variantNM_000404.4(GLB1):c.1113G>A (p.Lys371=)Mucopolysaccharidosis, MPS-IV-B [RCV003788122]likely benign33302428133024281Human1name
405045593CV3097199duplicationNM_000404.4(GLB1):c.560dup (p.Asn187fs)Mucopolysaccharidosis, MPS-IV-B [RCV003807779]pathogenic33305826133058262Human1name
405047579CV3097417single nucleotide variantNM_000404.4(GLB1):c.151A>C (p.Ile51Leu)Mucopolysaccharidosis, MPS-IV-B [RCV003807997]likely pathogenic33307263833072638Human1name
405048841CV3097510deletionNM_000404.4(GLB1):c.591del (p.Phe197fs)Mucopolysaccharidosis, MPS-IV-B [RCV003808090]pathogenic33305823133058231Human1name
405050336CV3097813single nucleotide variantNM_000404.4(GLB1):c.1056C>T (p.Asn352=)Mucopolysaccharidosis, MPS-IV-B [RCV003808226]likely benign33304613233046132Human1name
405001036CV3099255single nucleotide variantNM_000404.4(GLB1):c.1317C>T (p.Val439=)Mucopolysaccharidosis, MPS-IV-B [RCV003793676]likely benign33301847833018478Human1name
404979046CV3099325single nucleotide variantNM_000404.4(GLB1):c.1329A>T (p.Ala443=)Mucopolysaccharidosis, MPS-IV-B [RCV003791153]likely benign33301846633018466Human1name
404979652CV3099456single nucleotide variantNM_000404.4(GLB1):c.1692C>T (p.Asp564=)Mucopolysaccharidosis, MPS-IV-B [RCV003791284]likely benign33301409833014098Human1name
404980848CV3099660single nucleotide variantNM_000404.4(GLB1):c.148T>C (p.Tyr50His)Mucopolysaccharidosis, MPS-IV-B [RCV003791489]likely pathogenic33307264133072641Human1name
404981033CV3099692single nucleotide variantNM_000404.4(GLB1):c.1662G>A (p.Gly554=)Mucopolysaccharidosis, MPS-IV-B [RCV003791521]likely benign33301412833014128Human1name
405071281CV3099857single nucleotide variantNM_000404.4(GLB1):c.1350C>T (p.Ile450=)Mucopolysaccharidosis, MPS-IV-B [RCV003799572]likely benign33301683833016838Human1name
405074839CV3100220single nucleotide variantNM_000404.4(GLB1):c.1855C>T (p.Leu619=)Mucopolysaccharidosis, MPS-IV-B [RCV003799773]likely benign33299722432997224Human1name
405043256CV3101006single nucleotide variantNM_000404.4(GLB1):c.1083A>G (p.Pro361=)Mucopolysaccharidosis, MPS-IV-B [RCV003807706]likely benign33302431133024311Human1name
405153007CV3101974single nucleotide variantNM_000404.4(GLB1):c.1263A>C (p.Thr421=)Mucopolysaccharidosis, MPS-IV-B [RCV003801578]likely benign33301853233018532Human1name
405042673CV3103717single nucleotide variantNM_000404.4(GLB1):c.1812C>T (p.Pro604=)Mucopolysaccharidosis, MPS-IV-B [RCV003797435]likely benign33299726732997267Human1name
405168382CV3104114single nucleotide variantNM_000404.4(GLB1):c.1224G>A (p.Gln408=)Mucopolysaccharidosis, MPS-IV-B [RCV003802791]likely benign33302157533021575Human1name
405169742CV3104257single nucleotide variantNM_000404.4(GLB1):c.1842C>T (p.Asn614=)Mucopolysaccharidosis, MPS-IV-B [RCV003802934]likely benign33299723732997237Human1name
405037049CV3106259single nucleotide variantNM_000404.4(GLB1):c.1761C>T (p.Asn587=)Mucopolysaccharidosis, MPS-IV-B [RCV003796950]likely benign33299731832997318Human1name
405016084CV3106986single nucleotide variantNM_000404.4(GLB1):c.2016A>T (p.Ser672=)Mucopolysaccharidosis, MPS-IV-B [RCV003795156]likely benign33299706332997063Human1name
405055298CV3107866single nucleotide variantNM_000404.4(GLB1):c.1038G>A (p.Lys346=)Mucopolysaccharidosis, MPS-IV-B [RCV003808612]likely benign33304615033046150Human1name
405035858CV3108634duplicationNM_000404.4(GLB1):c.426dup (p.Glu143fs)Mucopolysaccharidosis, MPS-IV-B [RCV003807092]pathogenic33306826033068261Human1name
405161510CV3109874single nucleotide variantNM_000404.4(GLB1):c.1570C>T (p.Leu524=)Mucopolysaccharidosis, MPS-IV-B [RCV003802233]likely benign33301422033014220Human1name
405154075CV3111200single nucleotide variantNM_000404.4(GLB1):c.1500T>G (p.Thr500=)Mucopolysaccharidosis, MPS-IV-B [RCV003801656]likely benign33301429033014290Human1name
405070924CV3111378single nucleotide variantNM_000404.4(GLB1):c.1689A>G (p.Pro563=)Mucopolysaccharidosis, MPS-IV-B [RCV003809717]likely benign33301410133014101Human1name
405125528CV3111847single nucleotide variantNM_000404.4(GLB1):c.1911G>T (p.Thr637=)Mucopolysaccharidosis, MPS-IV-B [RCV003815320]likely benign33299716832997168Human1name
405108689CV3112363single nucleotide variantNM_000404.4(GLB1):c.1314A>G (p.Gly438=)Mucopolysaccharidosis, MPS-IV-B [RCV003813206]likely benign33301848133018481Human1name
405043676CV3112928single nucleotide variantNM_000404.4(GLB1):c.1584A>G (p.Gly528=)Mucopolysaccharidosis, MPS-IV-B [RCV003807595]likely benign33301420633014206Human1name
405081531CV3114898single nucleotide variantNM_000404.4(GLB1):c.1801T>C (p.Leu601=)Mucopolysaccharidosis, MPS-IV-B [RCV003810461]likely benign33299727832997278Human1name
405266111CV3201890single nucleotide variantNM_000404.4(GLB1):c.1584A>C (p.Gly528=)GLB1-related disorder [RCV004536893]likely benign33301420633014206Humanname , trait
407427324CV3410603single nucleotide variantNM_000404.4(GLB1):c.146G>C (p.Arg49Pro)GM1 gangliosidosis [RCV004586250]|GM1 gangliosidosis type 2 [RCV005023593]likely pathogenic33307264333072643Human2name , alternate_id
407477304CV3495095single nucleotide variantNM_000404.4(GLB1):c.101T>C (p.Ile34Thr)not specified [RCV004690997]uncertain significance33307268833072688Humanname
597638100CV3717462duplicationNM_000404.4(GLB1):c.488dup (p.Val164fs)GM1 gangliosidosis type 2 [RCV005024596]likely pathogenic33306552633065527Human1name , alternate_id
597638105CV3717463deletionNM_000404.4(GLB1):c.468del (p.Ala157fs)GM1 gangliosidosis type 2 [RCV005024597]likely pathogenic33306554733065547Human1name , alternate_id
597638123CV3717467single nucleotide variantNM_000404.4(GLB1):c.289C>T (p.Gln97Ter)GM1 gangliosidosis type 2 [RCV005024600]likely pathogenic33306892733068927Human1name , alternate_id
597638127CV3717468single nucleotide variantNM_000404.4(GLB1):c.288C>G (p.Tyr96Ter)GM1 gangliosidosis type 2 [RCV005024601]likely pathogenic33306892833068928Human1name , alternate_id
597716541CV3717469single nucleotide variantNM_000404.4(GLB1):c.275G>A (p.Trp92Ter)GM1 gangliosidosis type 2 [RCV005035308]pathogenic33306894133068941Human1name , alternate_id
597869014CV3869500single nucleotide variantNM_000404.4(GLB1):c.1428G>A (p.Leu476=)Mucopolysaccharidosis, MPS-IV-B [RCV005215431]likely benign33301676033016760Human1name
597857221CV3877769single nucleotide variantNM_000404.4(GLB1):c.1152A>C (p.Thr384=)Mucopolysaccharidosis, MPS-IV-B [RCV005229078]likely benign33302164733021647Human1name
597860490CV3879914single nucleotide variantNM_000404.4(GLB1):c.1029C>T (p.Leu343=)Mucopolysaccharidosis, MPS-IV-B [RCV005229494]likely benign33304615933046159Human1name
13515395CV488319single nucleotide variantNM_000404.4(GLB1):c.175C>T (p.Arg59Cys)GM1 gangliosidosis [RCV005240291]|GM1 gangliosidosis type 2 [RCV000669165]|GM1 gangliosidosis type 2 [RCV000987141]|Infantile GM1 gangliosidosis [RCV002245028]|Mucopolysaccharidosis, MPS-IV-B [RCV001050379]|not provided [RCV000597388]pathogenic|likely pathogenic33307261433072614Human4name , alternate_id
13532832CV511481single nucleotide variantNM_000404.4(GLB1):c.146G>A (p.Arg49His)GM1 gangliosidosis type 2 [RCV000672724]|Inborn genetic diseases [RCV000624583]|Mucopolysaccharidosis, MPS-IV-B [RCV001057694]|not provided [RCV003238787]pathogenic|likely pathogenic|uncertain significance|no classifications from unflagged records33307264333072643Human3name , alternate_id
13787902CV542962deletionNM_000404.4(GLB1):c.302del (p.Asp101fs)GM1 gangliosidosis type 2 [RCV000673695]likely pathogenic33306891433068914Human1name , alternate_id
13784633CV542965single nucleotide variantNM_000404.4(GLB1):c.248A>G (p.Tyr83Cys)GM1 gangliosidosis type 2 [RCV000671078]|Mucopolysaccharidosis, MPS-IV-B [RCV003767991]|Mucopolysaccharidosis, MPS-IV-B [RCV005240435]pathogenic|likely pathogenic|uncertain significance33306896833068968Human2name , alternate_id
13790068CV542967single nucleotide variantNM_000404.4(GLB1):c.188T>A (p.Phe63Tyr)GM1 gangliosidosis type 2 [RCV000674840]uncertain significance33307260133072601Human1name , alternate_id
13783641CV542970single nucleotide variantNM_000404.4(GLB1):c.152T>A (p.Ile51Asn)GM1 gangliosidosis type 2 [RCV000670208]|Mucopolysaccharidosis, MPS-IV-B [RCV003767982]pathogenic|uncertain significance33307263733072637Human2name , alternate_id
13791722CV543117duplicationNM_000404.4(GLB1):c.694dup (p.Ala232fs)GM1 gangliosidosis type 2 [RCV000667817]|Mucopolysaccharidosis, MPS-IV-B [RCV001048896]pathogenic|likely pathogenic33305812733058128Human2name , alternate_id
13786854CV543188deletionNM_000404.4(GLB1):c.846del (p.Thr283fs)GM1 gangliosidosis [RCV001175077]|GM1 gangliosidosis type 2 [RCV000673140]|GM1 gangliosidosis type 2 [RCV000987140]|Mucopolysaccharidosis, MPS-IV-B [RCV003768002]pathogenic33305195133051951Human3name , alternate_id
13788188CV543220deletionNM_000404.4(GLB1):c.626del (p.His209fs)GM1 gangliosidosis type 2 [RCV000673838]likely pathogenic33305819633058196Human1name , alternate_id
13831667CV582165single nucleotide variantNM_000404.4(GLB1):c.281G>A (p.Gly94Glu)Mucopolysaccharidosis, MPS-IV-B [RCV001862116]|not provided [RCV000722348]uncertain significance33306893533068935Human1name
14746718CV672008single nucleotide variantNM_000404.4(GLB1):c.253C>A (p.Pro85Thr)GM1 gangliosidosis type 2 [RCV000844884]uncertain significance33306896333068963Human1name
15138717CV691372single nucleotide variantNM_000404.4(GLB1):c.1938A>G (p.Ser646=)Mucopolysaccharidosis, MPS-IV-B [RCV000877204]likely benign33299714132997141Human1name
15133490CV691373single nucleotide variantNM_000404.4(GLB1):c.1833G>A (p.Ser611=)GLB1-related disorder [RCV004530845]|Mucopolysaccharidosis, MPS-IV-B [RCV000876321]|not provided [RCV001200662]benign|likely benign33299724632997246Human2name
15144480CV691374single nucleotide variantNM_000404.4(GLB1):c.1767C>T (p.Gly589=)Mucopolysaccharidosis, MPS-IV-B [RCV001434479]likely benign33299731232997312Human1name
15123020CV691375single nucleotide variantNM_000404.4(GLB1):c.1641G>A (p.Thr547=)Mucopolysaccharidosis, MPS-IV-B [RCV000874516]likely benign33301414933014149Human1name
15132742CV691376single nucleotide variantNM_000404.4(GLB1):c.1326A>G (p.Arg442=)Mucopolysaccharidosis, MPS-IV-B [RCV000876200]likely benign33301846933018469Human1name
15152889CV698038single nucleotide variantNM_000404.4(GLB1):c.1861C>T (p.Leu621=)Mucopolysaccharidosis, MPS-IV-B [RCV000945970]likely benign33299721832997218Human1name
15105246CV698040single nucleotide variantNM_000404.4(GLB1):c.1209C>G (p.Pro403=)Mucopolysaccharidosis, MPS-IV-B [RCV000959846]benign33302159033021590Human1name
15145510CV708787single nucleotide variantNM_000404.4(GLB1):c.1009C>T (p.Leu337=)Mucopolysaccharidosis, MPS-IV-B [RCV000967010]likely benign33304617933046179Human1name
15155078CV720405single nucleotide variantNM_000404.4(GLB1):c.1998G>A (p.Pro666=)Mucopolysaccharidosis, MPS-IV-B [RCV001485643]likely benign33299708132997081Human1name
15168180CV720406single nucleotide variantNM_000404.4(GLB1):c.1518C>T (p.Leu506=)Mucopolysaccharidosis, MPS-IV-B [RCV001479093]likely benign33301427233014272Human1name
15105623CV720407single nucleotide variantNM_000404.4(GLB1):c.1092T>C (p.Pro364=)Mucopolysaccharidosis, MPS-IV-B [RCV001503681]likely benign33302430233024302Human1name
15184979CV734026single nucleotide variantNM_000404.4(GLB1):c.2016A>G (p.Ser672=)GM1 gangliosidosis [RCV001150009]|GM1 gangliosidosis type 2 [RCV001563857]|GM1 gangliosidosis type 3 [RCV001563858]|Infantile GM1 gangliosidosis [RCV001563856]|Mucopolysaccharidosis, MPS-IV-B [RCV000908403]|Mucopolysaccharidosis, MPS-IV-B [RCV001150010]|not provided [RCV003438575]likely benign|uncertain significance33299706332997063Human5name , alternate_id
15138178CV734027single nucleotide variantNM_000404.4(GLB1):c.1830C>G (p.Thr610=)Mucopolysaccharidosis, MPS-IV-B [RCV000898934]likely benign33299724932997249Human1name
15167167CV734028single nucleotide variantNM_000404.4(GLB1):c.1644C>T (p.Leu548=)Mucopolysaccharidosis, MPS-IV-B [RCV002065724]likely benign33301414633014146Human1name
15133732CV748205single nucleotide variantNM_000404.4(GLB1):c.1356G>A (p.Gln452=)Mucopolysaccharidosis, MPS-IV-B [RCV001406460]likely benign33301683233016832Human1name
15193903CV748206single nucleotide variantNM_000404.4(GLB1):c.1122T>C (p.Tyr374=)Mucopolysaccharidosis, MPS-IV-B [RCV001858568]likely benign33302427233024272Human1name
15101715CV763816single nucleotide variantNM_000404.4(GLB1):c.1992A>G (p.Pro664=)Mucopolysaccharidosis, MPS-IV-B [RCV000936854]likely benign33299708732997087Human1name
15117396CV763817single nucleotide variantNM_000404.4(GLB1):c.1110A>G (p.Pro370=)Mucopolysaccharidosis, MPS-IV-B [RCV001481416]likely benign33302428433024284Human1name
15098637CV763818single nucleotide variantNM_000404.4(GLB1):c.1077A>G (p.Lys359=)Mucopolysaccharidosis, MPS-IV-B [RCV000936322]likely benign33302431733024317Human1name
28903323CV888670single nucleotide variantNM_000404.4(GLB1):c.1095C>T (p.Ile365=)GLB1-related disorder [RCV004538366]|GM1 gangliosidosis [RCV001143989]|Mucopolysaccharidosis, MPS-IV-B [RCV001143990]|Mucopolysaccharidosis, MPS-IV-B [RCV001506617]|not provided [RCV003438677]likely benign|uncertain significance33302429933024299Human2name
34891489CV906152single nucleotide variantNM_000404.4(GLB1):c.149A>G (p.Tyr50Cys)Infantile GM1 gangliosidosis [RCV001175103]|Mucopolysaccharidosis, MPS-IV-B [RCV001384625]pathogenic|uncertain significance33307264033072640Human2name , alternate_id
34895800CV916909deletionNM_000404.4(GLB1):c.699del (p.Gln234fs)GM1 gangliosidosis [RCV001192991]|GM1 gangliosidosis type 2 [RCV005029738]|Mucopolysaccharidosis, MPS-IV-B [RCV001859167]|not provided [RCV001268285]pathogenic|likely pathogenic33305812333058123Human3name , alternate_id
38461777CV943477single nucleotide variantNM_000404.4(GLB1):c.191A>G (p.Tyr64Cys)GM1 gangliosidosis type 2 [RCV005029800]|Inborn genetic diseases [RCV004978165]|Mucopolysaccharidosis, MPS-IV-B [RCV001231267]|not specified [RCV003235505]likely pathogenic|uncertain significance33307259833072598Human3name , alternate_id
8639821CV98804single nucleotide variantNM_000404.4(GLB1):c.1426C>T (p.Leu476=)GLB1-related disorder [RCV004537310]|GM1 gangliosidosis [RCV000382510]|Infantile GM1 gangliosidosis [RCV001449934]|Mucopolysaccharidosis, MPS-IV-B [RCV000327956]|Mucopolysaccharidosis, MPS-IV-B [RCV001082369]|not provided [RCV000078703]likely benign|conflicting interpretations of pathogenicity|uncertain significance33301676233016762Human3name , alternate_id
8639824CV98807single nucleotide variantNM_000404.4(GLB1):c.171C>G (p.Tyr57Ter)GM1 gangliosidosis [RCV003987350]|GM1 gangliosidosis type 2 [RCV000671504]|Mucopolysaccharidosis, MPS-IV-B [RCV002513824]|not provided [RCV000675686]pathogenic|likely pathogenic33307261833072618Human3name , alternate_id
8639826CV98809single nucleotide variantNM_000404.4(GLB1):c.1824G>C (p.Leu608=)GM1 gangliosidosis [RCV000406798]|Infantile GM1 gangliosidosis [RCV001527518]|Mucopolysaccharidosis, MPS-IV-B [RCV000288777]|Mucopolysaccharidosis, MPS-IV-B [RCV001512265]|not provided [RCV000675678]|not specified [RCV000078709]benign33299725532997255Human3name , alternate_id
126726270CV989480single nucleotide variantNM_000404.4(GLB1):c.218A>G (p.Lys73Arg)GM1 gangliosidosis type 3 [RCV001810021]|Mucopolysaccharidosis, MPS-IV-B [RCV001302836]uncertain significance33307257133072571Human2name
126767009CV1025207single nucleotide variantNM_000404.4(GLB1):c.845C>T (p.Ser282Phe)Mucopolysaccharidosis, MPS-IV-B [RCV001342649]uncertain significance33305195233051952Human1name
127254584CV1055331duplicationNM_000404.4(GLB1):c.2006dup (p.Asn669fs)GLB1-related disorder [RCV005232301]|GM1 gangliosidosis type 2 [RCV004796618]|Mucopolysaccharidosis, MPS-IV-B [RCV001379192]pathogenic|likely pathogenic33299707232997073Human3name
127246527CV1055332single nucleotide variantNM_000404.4(GLB1):c.557A>C (p.Glu186Ala)GM1 gangliosidosis [RCV001732176]|Mucopolysaccharidosis, MPS-IV-B [RCV001377615]likely pathogenic33305826533058265Human2name
127242728CV1059732single nucleotide variantNM_000404.4(GLB1):c.994G>A (p.Asp332Asn)GM1 gangliosidosis [RCV004690099]|GM1 gangliosidosis type 2 [RCV005038188]|Mucopolysaccharidosis, MPS-IV-B [RCV001383879]|not provided [RCV003327516]pathogenic33304619433046194Human3name , alternate_id
8574321CV106590duplicationNM_000404.4(GLB1):c.1188dup (p.Pro397fs)Infantile GM1 gangliosidosis [RCV000087091]pathogenic33302161033021611Human1name , alternate_id
8574322CV106592single nucleotide variantNM_000404.4(GLB1):c.922T>C (p.Phe308Leu)Infantile GM1 gangliosidosis [RCV000087093]pathogenic33305179133051791Human1name , alternate_id
127268660CV1092384single nucleotide variantNM_000404.4(GLB1):c.782A>G (p.Lys261Arg)GLB1-related disorder [RCV004533719]|Mucopolysaccharidosis, MPS-IV-B [RCV001430040]likely benign|uncertain significance33305350133053501Human2name
150451081CV1200418single nucleotide variantNM_000404.4(GLB1):c.821T>C (p.Leu274Pro)GM1 gangliosidosis type 2 [RCV001580715]|GM1 gangliosidosis type 3 [RCV001580716]|Infantile GM1 gangliosidosis [RCV001580714]|Mucopolysaccharidosis, MPS-IV-B [RCV001580717]uncertain significance33305197633051976Human4name , alternate_id
150521116CV1290180single nucleotide variantNM_000404.4(GLB1):c.451G>T (p.Asp151Tyr)GM1 gangliosidosis [RCV004798916]|Infantile GM1 gangliosidosis [RCV001730468]pathogenic|likely pathogenic33306823633068236Human2name , alternate_id
150547693CV1292127single nucleotide variantNM_000404.4(GLB1):c.998A>G (p.Tyr333Cys)GM1 gangliosidosis [RCV004798927]|GM1 gangliosidosis type 2 [RCV005038287]|Mucopolysaccharidosis, MPS-IV-B [RCV002290745]pathogenic|likely pathogenic33304619033046190Human3name , alternate_id
151348537CV1321053single nucleotide variantNM_000404.4(GLB1):c.808T>C (p.Tyr270His)Infantile GM1 gangliosidosis [RCV001803466]not provided33305198933051989Humanname , alternate_id
151348489CV1324054single nucleotide variantNM_000404.4(GLB1):c.884A>G (p.Asp295Gly)GM1 gangliosidosis type 3 [RCV001807967]|Mucopolysaccharidosis, MPS-IV-B [RCV002542425]uncertain significance33305191333051913Human2name
151811889CV1337403single nucleotide variantNM_000404.4(GLB1):c.850A>G (p.Ile284Val)Mucopolysaccharidosis, MPS-IV-B [RCV001943887]uncertain significance33305194733051947Human1name
151711786CV1338849duplicationNM_000404.4(GLB1):c.591dup (p.Asp198Ter)GM1 gangliosidosis type 2 [RCV002507682]|Infantile GM1 gangliosidosis [RCV002246614]|Mucopolysaccharidosis, MPS-IV-B [RCV002004514]pathogenic33305823033058231Human3name , alternate_id
151786540CV1345307single nucleotide variantNM_000404.4(GLB1):c.524A>G (p.Gln175Arg)Mucopolysaccharidosis, MPS-IV-B [RCV001893958]uncertain significance33306549133065491Human1name
8659647CV134600single nucleotide variantNM_000404.4(GLB1):c.325C>T (p.Arg109Trp)GM1 gangliosidosis [RCV000372110]|Mucopolysaccharidosis, MPS-IV-B [RCV000338369]|Mucopolysaccharidosis, MPS-IV-B [RCV001522631]|not provided [RCV000675685]|not specified [RCV000117143]benign|likely benign|conflicting interpretations of pathogenicity33306889133068891Human2name
151720399CV1350291single nucleotide variantNM_000404.4(GLB1):c.517C>G (p.Leu173Val)Mucopolysaccharidosis, MPS-IV-B [RCV002036528]likely pathogenic33306549833065498Human1name
151720417CV1359753single nucleotide variantNM_000404.4(GLB1):c.905G>T (p.Ser302Ile)Mucopolysaccharidosis, MPS-IV-B [RCV002036570]uncertain significance33305189233051892Human1name
151809806CV1366982deletionNM_000404.4(GLB1):c.1142del (p.Lys381fs)GM1 gangliosidosis type 2 [RCV002307812]|Mucopolysaccharidosis, MPS-IV-B [RCV001939477]pathogenic|likely pathogenic33302425233024252Human2name , alternate_id
151819558CV1384282single nucleotide variantNM_000404.4(GLB1):c.625C>T (p.His209Tyr)Mucopolysaccharidosis, MPS-IV-B [RCV001960487]uncertain significance33305819733058197Human1name
151794454CV1387175single nucleotide variantNM_000404.4(GLB1):c.703G>A (p.Gly235Ser)Mucopolysaccharidosis, MPS-IV-B [RCV001910397]uncertain significance33305811933058119Human1name
151712004CV1391338deletionNM_000404.4(GLB1):c.2006del (p.Asn669fs)Mucopolysaccharidosis, MPS-IV-B [RCV002005262]uncertain significance33299707332997073Human1name
151825282CV1393678deletionNM_000404.4(GLB1):c.1310del (p.Asn437fs)Mucopolysaccharidosis, MPS-IV-B [RCV001972704]pathogenic33301848533018485Human1name
151810132CV1397009single nucleotide variantNM_000404.4(GLB1):c.779C>A (p.Pro260His)Mucopolysaccharidosis, MPS-IV-B [RCV001940305]uncertain significance33305350433053504Human1name
151803373CV1415894single nucleotide variantNM_000404.4(GLB1):c.424A>T (p.Lys142Ter)Mucopolysaccharidosis, MPS-IV-B [RCV001927524]pathogenic33306826333068263Human1name
151768560CV1421164single nucleotide variantNM_000404.4(GLB1):c.569G>A (p.Gly190Asp)Infantile GM1 gangliosidosis [RCV002290779]|Mucopolysaccharidosis, MPS-IV-B [RCV001863251]|Mucopolysaccharidosis, MPS-IV-B [RCV004782800]pathogenic|likely pathogenic33305825333058253Human2name , alternate_id
151788434CV1422517single nucleotide variantNM_000404.4(GLB1):c.982C>T (p.Pro328Ser)Mucopolysaccharidosis, MPS-IV-B [RCV001898423]|not specified [RCV003317543]pathogenic|uncertain significance33304620633046206Human1name
151716806CV1433853single nucleotide variantNM_000404.4(GLB1):c.521A>C (p.Tyr174Ser)Mucopolysaccharidosis, MPS-IV-B [RCV002024552]likely pathogenic33306549433065494Human1name
151710824CV1439019single nucleotide variantNM_000404.4(GLB1):c.397G>T (p.Gly133Ter)Mucopolysaccharidosis, MPS-IV-B [RCV001999719]pathogenic33306829033068290Human1name
151718483CV1452917single nucleotide variantNM_000404.4(GLB1):c.836A>G (p.Gln279Arg)Mucopolysaccharidosis, MPS-IV-B [RCV002030195]uncertain significance33305196133051961Human1name
151796072CV1453775single nucleotide variantNM_000404.4(GLB1):c.586G>C (p.Asp196His)Mucopolysaccharidosis, MPS-IV-B [RCV001913261]uncertain significance33305823633058236Human1name
151711130CV1468323single nucleotide variantNM_000404.4(GLB1):c.380G>T (p.Cys127Phe)GM1 gangliosidosis type 2 [RCV005025590]|Mucopolysaccharidosis, MPS-IV-B [RCV002001035]|not specified [RCV004526893]likely pathogenic|uncertain significance33306883633068836Human2name , alternate_id
151721303CV1472922single nucleotide variantNM_000404.4(GLB1):c.751G>A (p.Ala251Thr)Mucopolysaccharidosis, MPS-IV-B [RCV002039498]uncertain significance33305353233053532Human1name
151807672CV1480418duplicationNM_000404.4(GLB1):c.1336dup (p.Ala446fs)Mucopolysaccharidosis, MPS-IV-B [RCV001935176]pathogenic33301845833018459Human1name
151794310CV1500261single nucleotide variantNM_000404.4(GLB1):c.956G>A (p.Gly319Glu)Mucopolysaccharidosis, MPS-IV-B [RCV001910040]uncertain significance33304623233046232Human1name
151825695CV1503667single nucleotide variantNM_000404.4(GLB1):c.451G>A (p.Asp151Asn)Mucopolysaccharidosis, MPS-IV-B [RCV001973484]likely pathogenic33306823633068236Human1name
151716071CV1504264single nucleotide variantNM_000404.4(GLB1):c.712A>G (p.Thr238Ala)Mucopolysaccharidosis, MPS-IV-B [RCV002022369]uncertain significance33305811033058110Human1name
8595217CV15964single nucleotide variantNM_000404.4(GLB1):c.601C>T (p.Arg201Cys)GLB1-related disorder [RCV004737133]|GM1 gangliosidosis [RCV000269582]|GM1 gangliosidosis type 2 [RCV000000973]|GM1 gangliosidosis type 2 [RCV005024979]|GM1 gangliosidosis type 3 [RCV000410436]|Infantile GM1 gangliosidosis [RCV000411359]|Mucopolysaccharidosis, Mpathogenic|likely pathogenic|uncertain significance33305822133058221Human5name , alternate_id
8595219CV15967single nucleotide variantNM_000404.4(GLB1):c.367G>A (p.Gly123Arg)Infantile GM1 gangliosidosis [RCV000000976]|Mucopolysaccharidosis, MPS-IV-B [RCV001217770]|Mucopolysaccharidosis, MPS-IV-B [RCV004799724]|not provided [RCV000428850]pathogenic|likely pathogenic33306884933068849Human2name , alternate_id
8595220CV15968single nucleotide variantNM_000404.4(GLB1):c.947A>G (p.Tyr316Cys)GM1 gangliosidosis type 2 [RCV000673295]|Infantile GM1 gangliosidosis [RCV000000977]pathogenic|likely pathogenic33305176633051766Human2name , alternate_id
8595222CV15970single nucleotide variantNM_000404.4(GLB1):c.818G>T (p.Trp273Leu)Infantile GM1 gangliosidosis [RCV004566665]|Mucopolysaccharidosis, MPS-IV-B [RCV000000979]pathogenic|likely pathogenic33305197933051979Human2name , alternate_id
8595227CV15978single nucleotide variantNM_000404.4(GLB1):c.622C>T (p.Arg208Cys)GM1 gangliosidosis [RCV000586182]|GM1 gangliosidosis type 2 [RCV000984269]|GM1 gangliosidosis type 2 [RCV005024980]|GM1 gangliosidosis type 3 [RCV000984270]|Inborn genetic diseases [RCV002512629]|Infantile GM1 gangliosidosis [RCV000000988]|Mucopolysaccharidosis, MPS-IV-B [RCV000633470]|Mucopolysacchpathogenic33305820033058200Human6name , alternate_id
153303511CV1686301single nucleotide variantNM_000404.4(GLB1):c.944C>A (p.Ala315Asp)Inborn genetic diseases [RCV003095896]|Mucopolysaccharidosis, MPS-IV-B [RCV003095895]|not provided [RCV002261734]uncertain significance33305176933051769Human2name
153303512CV1686302single nucleotide variantNM_000404.4(GLB1):c.377T>C (p.Ile126Thr)not provided [RCV002261735]uncertain significance33306883933068839Humanname
153345836CV1691466single nucleotide variantNM_000404.4(GLB1):c.390G>A (p.Trp130Ter)GM1 gangliosidosis [RCV002272949]pathogenic33306882633068826Human1name
153346594CV1691877duplicationNM_000404.4(GLB1):c.2010dup (p.Asp671fs)Infantile GM1 gangliosidosis [RCV002273360]uncertain significance33299706832997069Human1name , alternate_id
155644270CV1708527single nucleotide variantNM_000404.4(GLB1):c.569G>T (p.Gly190Val)Infantile GM1 gangliosidosis [RCV002291070]likely pathogenic33305825333058253Human1name , alternate_id
9692974CV177089single nucleotide variantNM_000404.4(GLB1):c.901G>A (p.Ala301Thr)not provided [RCV000180156]likely pathogenic33305189633051896Humanname
155671985CV1773961single nucleotide variantNM_000404.4(GLB1):c.838C>G (p.Pro280Ala)Mucopolysaccharidosis, MPS-IV-B [RCV002297532]uncertain significance33305195933051959Human1name
9692972CV177750deletionNM_000404.4(GLB1):c.1077del (p.Val360fs)GM1 gangliosidosis [RCV002470776]|Infantile GM1 gangliosidosis [RCV002291499]|Mucopolysaccharidosis, MPS-IV-B [RCV001035980]|Mucopolysaccharidosis, MPS-IV-B [RCV001192990]|not provided [RCV000173999]pathogenic33302431733024317Human3name , alternate_id
155949268CV1869358single nucleotide variantNM_000404.4(GLB1):c.467C>T (p.Ala156Val)Mucopolysaccharidosis, MPS-IV-B [RCV003074048]uncertain significance33306554833065548Human1name
156387666CV1875684single nucleotide variantNM_000404.4(GLB1):c.581C>T (p.Ala194Val)Mucopolysaccharidosis, MPS-IV-B [RCV003050999]uncertain significance33305824133058241Human1name
156289635CV1881717single nucleotide variantNM_000404.4(GLB1):c.938A>G (p.Asn313Ser)Mucopolysaccharidosis, MPS-IV-B [RCV003061397]pathogenic33305177533051775Human1name
156048143CV1884224single nucleotide variantNM_000404.4(GLB1):c.838C>T (p.Pro280Ser)Mucopolysaccharidosis, MPS-IV-B [RCV003078771]uncertain significance33305195933051959Human1name
156352379CV1893280single nucleotide variantNM_000404.4(GLB1):c.482G>A (p.Trp161Ter)Mucopolysaccharidosis, MPS-IV-B [RCV003091081]pathogenic33306553333065533Human1name
156399770CV1897479single nucleotide variantNM_000404.4(GLB1):c.842A>G (p.His281Arg)Mucopolysaccharidosis, MPS-IV-B [RCV002584751]|not specified [RCV005406592]likely pathogenic|uncertain significance33305195533051955Human1name
156134870CV1905659single nucleotide variantNM_000404.4(GLB1):c.617G>A (p.Arg206His)Mucopolysaccharidosis, MPS-IV-B [RCV003081976]uncertain significance33305820533058205Human1name
156361204CV1925546single nucleotide variantNM_000404.4(GLB1):c.785G>T (p.Gly262Val)Mucopolysaccharidosis, MPS-IV-B [RCV002651651]pathogenic33305349833053498Human1name
156361219CV1925547single nucleotide variantNM_000404.4(GLB1):c.785G>A (p.Gly262Glu)GM1 gangliosidosis [RCV005239709]|Mucopolysaccharidosis, MPS-IV-B [RCV002651652]pathogenic|likely pathogenic33305349833053498Human2name
156162395CV1925548single nucleotide variantNM_000404.4(GLB1):c.304C>G (p.His102Asp)Mucopolysaccharidosis, MPS-IV-B [RCV002664299]pathogenic33306891233068912Human1name
156380035CV1927466single nucleotide variantNM_000404.4(GLB1):c.895C>T (p.Arg299Cys)Mucopolysaccharidosis, MPS-IV-B [RCV002634196]|not provided [RCV004695318]uncertain significance33305190233051902Human1name
156311474CV1934309single nucleotide variantNM_000404.4(GLB1):c.326G>A (p.Arg109Gln)Mucopolysaccharidosis, MPS-IV-B [RCV002629797]uncertain significance33306889033068890Human1name
156437339CV1937479single nucleotide variantNM_000404.4(GLB1):c.592G>C (p.Asp198His)Mucopolysaccharidosis, MPS-IV-B [RCV003106873]uncertain significance33305823033058230Human1name
10048960CV195238single nucleotide variantNM_000404.4(GLB1):c.602G>A (p.Arg201His)GM1 gangliosidosis [RCV000309607]|GM1 gangliosidosis type 2 [RCV000995553]|GM1 gangliosidosis type 2 [RCV002500509]|Infantile GM1 gangliosidosis [RCV002286710]|Mucopolysaccharidosis, MPS-IV-B [RCV000665698]|Mucopolysaccharidosis, MPS-IV-B [RCV000818052]|not provided [RCV000255006]pathogenic|likely pathogenic33305822033058220Human4name , alternate_id
10049153CV195887single nucleotide variantNM_000404.4(GLB1):c.809A>G (p.Tyr270Cys)Mucopolysaccharidosis, MPS-IV-B [RCV001852241]|not provided [RCV000180154]|not specified [RCV003155108]likely pathogenic|uncertain significance33305198833051988Human1name
10053168CV195888single nucleotide variantNM_000404.4(GLB1):c.809A>C (p.Tyr270Ser)not provided [RCV000180159]uncertain significance33305198833051988Humanname
156419993CV1979331single nucleotide variantNM_000404.4(GLB1):c.915G>C (p.Leu305Phe)Mucopolysaccharidosis, MPS-IV-B [RCV002613242]uncertain significance33305179833051798Human1name
10056022CV198618duplicationNM_000404.4(GLB1):c.1577dup (p.Trp527fs)GLB1-related disorder [RCV004528961]|GM1 gangliosidosis [RCV001260322]|GM1 gangliosidosis type 2 [RCV000987139]|GM1 gangliosidosis type 2 [RCV005025294]|GM1 gangliosidosis type 3 [RCV003137707]|Infantile GM1 gangliosidosis [RCV000184037]|Mucopolysaccharidosis, Mpathogenic|likely pathogenic|not provided33301421233014213Human5name , alternate_id
156385681CV1998047single nucleotide variantNM_000404.4(GLB1):c.905G>A (p.Ser302Asn)Mucopolysaccharidosis, MPS-IV-B [RCV002653974]uncertain significance33305189233051892Human1name
156138006CV2006474single nucleotide variantNM_000404.4(GLB1):c.357C>G (p.Ile119Met)Mucopolysaccharidosis, MPS-IV-B [RCV002663463]uncertain significance33306885933068859Human1name
155907954CV2017422single nucleotide variantNM_000404.4(GLB1):c.937A>G (p.Asn313Asp)Mucopolysaccharidosis, MPS-IV-B [RCV002681511]likely pathogenic33305177633051776Human1name
156059704CV2034463single nucleotide variantNM_000404.4(GLB1):c.905G>C (p.Ser302Thr)Mucopolysaccharidosis, MPS-IV-B [RCV002736794]uncertain significance33305189233051892Human1name
155933020CV2035185single nucleotide variantNM_000404.4(GLB1):c.670C>G (p.His224Asp)Mucopolysaccharidosis, MPS-IV-B [RCV002751266]uncertain significance33305815233058152Human1name
156336988CV2057822single nucleotide variantNM_000404.4(GLB1):c.837A>C (p.Gln279His)Mucopolysaccharidosis, MPS-IV-B [RCV002810993]uncertain significance33305196033051960Human1name
156322580CV2067708single nucleotide variantNM_000404.4(GLB1):c.806T>C (p.Phe269Ser)Mucopolysaccharidosis, MPS-IV-B [RCV002834805]uncertain significance33305199133051991Human1name
156218612CV2087470duplicationNM_000404.4(GLB1):c.1654dup (p.Tyr552fs)Mucopolysaccharidosis, MPS-IV-B [RCV002875777]pathogenic33301413533014136Human1name
156340205CV2106929single nucleotide variantNM_000404.4(GLB1):c.623G>T (p.Arg208Leu)Mucopolysaccharidosis, MPS-IV-B [RCV002938855]uncertain significance33305819933058199Human1name
156321161CV2112028deletionNM_000404.4(GLB1):c.1417del (p.Leu473fs)Mucopolysaccharidosis, MPS-IV-B [RCV002937759]pathogenic33301677133016771Human1name
156036679CV2143240single nucleotide variantNM_000404.4(GLB1):c.697C>A (p.Leu233Met)Mucopolysaccharidosis, MPS-IV-B [RCV002999358]uncertain significance33305812533058125Human1name
155960650CV2144211single nucleotide variantNM_000404.4(GLB1):c.911A>G (p.Asn304Ser)Mucopolysaccharidosis, MPS-IV-B [RCV003015447]uncertain significance33305188633051886Human1name
156178633CV2144935single nucleotide variantNM_000404.4(GLB1):c.802G>C (p.Glu268Gln)Mucopolysaccharidosis, MPS-IV-B [RCV003005635]pathogenic33305199533051995Human1name
156309498CV2150192single nucleotide variantNM_000404.4(GLB1):c.454C>A (p.Pro152Thr)Mucopolysaccharidosis, MPS-IV-B [RCV003028494]uncertain significance33306823333068233Human1name
156372063CV2174686single nucleotide variantNM_000404.4(GLB1):c.331G>A (p.Ala111Thr)Mucopolysaccharidosis, MPS-IV-B [RCV003049785]uncertain significance33306888533068885Human1name
156338893CV2179605single nucleotide variantNM_000404.4(GLB1):c.932G>A (p.Gly311Glu)Mucopolysaccharidosis, MPS-IV-B [RCV003030175]likely pathogenic33305178133051781Human1name
156040838CV2187915single nucleotide variantNM_000404.4(GLB1):c.774T>A (p.Cys258Ter)Mucopolysaccharidosis, MPS-IV-B [RCV003036562]pathogenic33305350933053509Human1name
156434510CV2402969single nucleotide variantNM_000404.4(GLB1):c.713C>T (p.Thr238Ile)GM1 gangliosidosis type 2 [RCV003126397]uncertain significance33305810933058109Human1name
11545225CV251093single nucleotide variantNM_000404.4(GLB1):c.915G>T (p.Leu305Phe)not specified [RCV000244846]likely benign33305179833051798Humanname
11560287CV259759single nucleotide variantNM_000404.4(GLB1):c.464T>G (p.Leu155Arg)GM1 gangliosidosis type 2 [RCV000665871]|Infantile GM1 gangliosidosis [RCV001175291]|Mucopolysaccharidosis, MPS-IV-B [RCV000809706]|Mucopolysaccharidosis, MPS-IV-B [RCV000984003]|not provided [RCV000256106]pathogenic|likely pathogenic|not provided33306555133065551Human3name , alternate_id
11641469CV265262single nucleotide variantNM_000404.4(GLB1):c.385G>A (p.Glu129Lys)not provided [RCV000357258]uncertain significance33306883133068831Humanname
401719751CV2672012single nucleotide variantNM_000404.4(GLB1):c.562G>T (p.Glu188Ter)Infantile GM1 gangliosidosis [RCV003238167]|Mucopolysaccharidosis, MPS-IV-B [RCV003779865]pathogenic33305826033058260Human2name , alternate_id
11637557CV268408single nucleotide variantNM_000404.4(GLB1):c.647T>C (p.Val216Ala)not provided [RCV000288015]uncertain significance33305817533058175Humanname
11580888CV268409single nucleotide variantNM_000404.4(GLB1):c.808T>G (p.Tyr270Asp)GLB1-related disorder [RCV004545765]|GM1 gangliosidosis type 2 [RCV000666452]|Inborn genetic diseases [RCV000623067]|Mucopolysaccharidosis, MPS-IV-B [RCV000689244]|Mucopolysaccharidosis, MPS-IV-B [RCV000780303]|not provided [RCV000394616]pathogenic|likely pathogenic|not provided33305198933051989Human6name , alternate_id
401855768CV2753134single nucleotide variantNM_000404.4(GLB1):c.739A>G (p.Asn247Asp)Infantile GM1 gangliosidosis [RCV003338190]uncertain significance33305354433053544Human1name , alternate_id
401917153CV2829690single nucleotide variantNM_000404.4(GLB1):c.825T>A (p.Asp275Glu)not provided [RCV003443734]uncertain significance33305197233051972Humanname
11648281CV290020single nucleotide variantNM_000404.4(GLB1):c.376A>G (p.Ile126Val)GM1 gangliosidosis [RCV000387505]|Mucopolysaccharidosis, MPS-IV-B [RCV000281036]|Mucopolysaccharidosis, MPS-IV-B [RCV000809497]uncertain significance33306884033068840Human2name
402525151CV3086752single nucleotide variantNM_000404.4(GLB1):c.710A>G (p.Tyr237Cys)GM1 gangliosidosis type 2 [RCV005030265]|Mucopolysaccharidosis, MPS-IV-B [RCV003781369]pathogenic|likely pathogenic33305811233058112Human2name , alternate_id
402524723CV3086753single nucleotide variantNM_000404.4(GLB1):c.550C>T (p.Gln184Ter)Mucopolysaccharidosis, MPS-IV-B [RCV003781370]pathogenic33306546533065465Human1name
404991203CV3091280single nucleotide variantNM_000404.4(GLB1):c.517C>T (p.Leu173Phe)Mucopolysaccharidosis, MPS-IV-B [RCV003792753]likely pathogenic33306549833065498Human1name
405001254CV3095470single nucleotide variantNM_000404.4(GLB1):c.443G>T (p.Arg148Leu)Mucopolysaccharidosis, MPS-IV-B [RCV003793773]|not specified [RCV004767466]likely pathogenic|uncertain significance33306824433068244Human1name
405047645CV3097422deletionNM_000404.4(GLB1):c.1577del (p.Gly526fs)Mucopolysaccharidosis, MPS-IV-B [RCV003808002]pathogenic33301421333014213Human1name
405028529CV3098176single nucleotide variantNM_000404.4(GLB1):c.765G>T (p.Gln255His)Mucopolysaccharidosis, MPS-IV-B [RCV003806469]likely pathogenic33305351833053518Human1name
405178400CV3101556single nucleotide variantNM_000404.4(GLB1):c.572G>C (p.Ser191Thr)Mucopolysaccharidosis, MPS-IV-B [RCV003803769]|not specified [RCV005407256]likely pathogenic|uncertain significance33305825033058250Human1name
405109751CV3112559deletionNM_000404.4(GLB1):c.1583del (p.Gly528fs)Mucopolysaccharidosis, MPS-IV-B [RCV003813402]pathogenic33301420733014207Human1name
405043611CV3112933single nucleotide variantNM_000404.4(GLB1):c.520T>G (p.Tyr174Asp)Mucopolysaccharidosis, MPS-IV-B [RCV003807600]likely pathogenic33306549533065495Human1name
405106640CV3113664single nucleotide variantNM_000404.4(GLB1):c.572G>T (p.Ser191Ile)Mucopolysaccharidosis, MPS-IV-B [RCV003812786]likely pathogenic33305825033058250Human1name
405012751CV3114187single nucleotide variantNM_000404.4(GLB1):c.971A>C (p.Tyr324Ser)Mucopolysaccharidosis, MPS-IV-B [RCV003805041]likely pathogenic33304621733046217Human1name
407428600CV3410292single nucleotide variantNM_000404.4(GLB1):c.998A>T (p.Tyr333Phe)not specified [RCV004587899]uncertain significance33304619033046190Humanname
407573331CV3499133single nucleotide variantNM_000404.4(GLB1):c.887T>C (p.Ile296Thr)not specified [RCV004700105]uncertain significance33305191033051910Humanname
12742249CV359418single nucleotide variantNM_000404.4(GLB1):c.841C>T (p.His281Tyr)GLB1-related disorder [RCV004737460]|Mucopolysaccharidosis, MPS-IV-B [RCV000662341]|Mucopolysaccharidosis, MPS-IV-B [RCV000805468]|Mucopolysaccharidosis, MPS-IV-B [RCV005410898]|not provided [RCV000413217]pathogenic|likely pathogenic|not provided33305195633051956Human3name , alternate_id
12848811CV368399single nucleotide variantNM_000404.4(GLB1):c.902C>T (p.Ala301Val)GLB1-related disorder [RCV004532999]|GM1 gangliosidosis [RCV003330669]|Mucopolysaccharidosis, MPS-IV-B [RCV000670128]|Mucopolysaccharidosis, MPS-IV-B [RCV001244569]|not provided [RCV000418628]pathogenic|likely pathogenic33305189533051895Human2name
597638082CV3717459deletionNM_000404.4(GLB1):c.1242del (p.Phe415fs)GM1 gangliosidosis type 2 [RCV005024593]likely pathogenic33301855333018553Human1name , alternate_id
597638111CV3717465single nucleotide variantNM_000404.4(GLB1):c.462C>G (p.Tyr154Ter)GM1 gangliosidosis type 2 [RCV005024598]likely pathogenic33306555333065553Human1name , alternate_id
597655593CV3731497single nucleotide variantNM_000404.4(GLB1):c.376A>C (p.Ile126Leu)not provided [RCV005001678]uncertain significance33306884033068840Humanname
597852827CV3870119single nucleotide variantNM_000404.4(GLB1):c.718G>A (p.Val240Met)Mucopolysaccharidosis, MPS-IV-B [RCV005228511]pathogenic33305810433058104Human1name
597852835CV3870120single nucleotide variantNM_000404.4(GLB1):c.452A>T (p.Asp151Val)Mucopolysaccharidosis, MPS-IV-B [RCV005228512]pathogenic33306823533068235Human1name
597852845CV3870121single nucleotide variantNM_000404.4(GLB1):c.400G>A (p.Gly134Arg)Mucopolysaccharidosis, MPS-IV-B [RCV005228513]pathogenic33306828733068287Human1name
597835679CV3874256single nucleotide variantNM_000404.4(GLB1):c.668C>G (p.Ala223Gly)Mucopolysaccharidosis, MPS-IV-B [RCV005210176]uncertain significance33305815433058154Human1name
597925098CV3877401single nucleotide variantNM_000404.4(GLB1):c.835C>T (p.Gln279Ter)Mucopolysaccharidosis, MPS-IV-B [RCV005224097]pathogenic33305196233051962Human1name
597841694CV3878122single nucleotide variantNM_000404.4(GLB1):c.521A>G (p.Tyr174Cys)Mucopolysaccharidosis, MPS-IV-B [RCV005226609]likely pathogenic33306549433065494Human1name
598125945CV3883368single nucleotide variantNM_000404.4(GLB1):c.859G>T (p.Glu287Ter)GM1 gangliosidosis type 2 [RCV005233239]likely pathogenic33305193833051938Human1name
598126004CV3883413single nucleotide variantNM_000404.4(GLB1):c.890T>G (p.Leu297Arg)Infantile GM1 gangliosidosis [RCV005233282]not provided33305190733051907Humanname , alternate_id
598122711CV3884643single nucleotide variantNM_000404.4(GLB1):c.391G>A (p.Glu131Lys)not specified [RCV005237335]uncertain significance33306882533068825Humanname
598123014CV3884657single nucleotide variantNM_000404.4(GLB1):c.363G>T (p.Arg121Ser)not specified [RCV005238263]uncertain significance33306885333068853Humanname
598124943CV3885487single nucleotide variantNM_000404.4(GLB1):c.787C>T (p.Pro263Ser)GM1 gangliosidosis [RCV005240065]likely pathogenic33305349633053496Human1name
598122483CV3889887single nucleotide variantNM_000404.4(GLB1):c.326G>C (p.Arg109Pro)Infantile GM1 gangliosidosis [RCV005247990]uncertain significance33306889033068890Human1name , alternate_id
617151852CV4018194single nucleotide variantNM_000404.4(GLB1):c.819G>T (p.Trp273Cys)not specified [RCV005418454]uncertain significance33305197833051978Humanname
617153385CV4018549single nucleotide variantNM_000404.4(GLB1):c.520T>C (p.Tyr174His)Mucopolysaccharidosis, MPS-IV-B [RCV005418810]likely pathogenic33306549533065495Human1name
13527921CV513262single nucleotide variantNM_000404.4(GLB1):c.439C>T (p.Leu147Phe)Infantile GM1 gangliosidosis [RCV000625810]|Mucopolysaccharidosis, MPS-IV-B [RCV002295308]likely pathogenic|uncertain significance33306824833068248Human2name , alternate_id
13528663CV513535single nucleotide variantNM_000404.4(GLB1):c.443G>A (p.Arg148His)GM1 gangliosidosis type 2 [RCV000763097]|Mucopolysaccharidosis, MPS-IV-B [RCV000626074]|Mucopolysaccharidosis, MPS-IV-B [RCV001855325]pathogenic|likely pathogenic33306824433068244Human2name , alternate_id
13789429CV542929deletionNM_000404.4(GLB1):c.1991del (p.Pro664fs)GM1 gangliosidosis type 2 [RCV000665992]likely pathogenic|conflicting interpretations of pathogenicity|uncertain significance33299708832997088Human1name , alternate_id
13784339CV542939single nucleotide variantNM_000404.4(GLB1):c.797A>G (p.Asn266Ser)GM1 gangliosidosis type 2 [RCV000670767]uncertain significance33305200033052000Human1name , alternate_id
13786941CV542944single nucleotide variantNM_000404.4(GLB1):c.572G>A (p.Ser191Asn)GM1 gangliosidosis type 2 [RCV000664551]|Mucopolysaccharidosis, MPS-IV-B [RCV002530631]pathogenic|uncertain significance33305825033058250Human2name , alternate_id
13785542CV542960single nucleotide variantNM_000404.4(GLB1):c.401G>T (p.Gly134Val)GM1 gangliosidosis type 2 [RCV000672112]|Mucopolysaccharidosis, MPS-IV-B [RCV002531304]pathogenic|uncertain significance33306828633068286Human2name , alternate_id
13788011CV543109duplicationNM_000404.4(GLB1):c.1634dup (p.Asn545fs)GM1 gangliosidosis type 2 [RCV000665150]|Mucopolysaccharidosis, MPS-IV-B [RCV001380450]pathogenic|likely pathogenic33301415533014156Human2name , alternate_id
13787134CV543156deletionNM_000404.4(GLB1):c.2011del (p.Asp671fs)GM1 gangliosidosis type 2 [RCV000673292]uncertain significance33299706832997068Human1name , alternate_id
13784107CV543192single nucleotide variantNM_000404.4(GLB1):c.765G>C (p.Gln255His)GM1 gangliosidosis type 2 [RCV000670551]|Mucopolysaccharidosis, MPS-IV-B [RCV003767987]likely pathogenic33305351833053518Human2name , alternate_id
13790933CV543207single nucleotide variantNM_000404.4(GLB1):c.442C>A (p.Arg148Ser)GLB1-related disorder [RCV004533467]|GM1 gangliosidosis [RCV001175301]|GM1 gangliosidosis type 2 [RCV000666897]|Mucopolysaccharidosis, MPS-IV-B [RCV000780304]|Mucopolysaccharidosis, MPS-IV-B [RCV001055679]|not provided [RCV000727559]pathogenic|likely pathogenic|not provided33306824533068245Human5name , alternate_id
13786267CV543219single nucleotide variantNM_000404.4(GLB1):c.971A>G (p.Tyr324Cys)GM1 gangliosidosis type 2 [RCV000672690]|Mucopolysaccharidosis, MPS-IV-B [RCV003767999]likely pathogenic|uncertain significance33304621733046217Human2name , alternate_id
13789910CV543222single nucleotide variantNM_000404.4(GLB1):c.523C>T (p.Gln175Ter)GM1 gangliosidosis type 2 [RCV000666243]likely pathogenic33306549233065492Human1name , alternate_id
13792350CV543223single nucleotide variantNM_000404.4(GLB1):c.446C>T (p.Ser149Phe)GM1 gangliosidosis type 2 [RCV000668601]|GM1 gangliosidosis type 2 [RCV000679994]|Mucopolysaccharidosis, MPS-IV-B [RCV001228044]|Mucopolysaccharidosis, MPS-IV-B [RCV005407863]pathogenic|uncertain significance|no classifications from unflagged records33306824133068241Human2name , alternate_id
13786569CV543242single nucleotide variantNM_000404.4(GLB1):c.395T>C (p.Met132Thr)GM1 gangliosidosis type 2 [RCV000672923]|Infantile GM1 gangliosidosis [RCV002249399]|Mucopolysaccharidosis, MPS-IV-B [RCV001731879]pathogenic|likely pathogenic|uncertain significance33306882133068821Human3name , alternate_id
13784343CV543243single nucleotide variantNM_000404.4(GLB1):c.335A>C (p.His112Pro)GM1 gangliosidosis [RCV005056415]|GM1 gangliosidosis type 2 [RCV000670769]|Mucopolysaccharidosis, MPS-IV-B [RCV002531261]pathogenic|likely pathogenic|uncertain significance33306888133068881Human3name , alternate_id
13794640CV553376single nucleotide variantNM_000404.4(GLB1):c.623G>A (p.Arg208His)GM1 gangliosidosis [RCV001148903]|Mucopolysaccharidosis, MPS-IV-B [RCV000876207]|Mucopolysaccharidosis, MPS-IV-B [RCV001145887]|not provided [RCV001354677]likely benign|conflicting interpretations of pathogenicity|uncertain significance33305819933058199Human2name
13832118CV582609deletionNM_000404.4(GLB1):c.1191del (p.Ile398fs)Mucopolysaccharidosis, MPS-IV-B [RCV001868921]|not provided [RCV000722801]pathogenic|uncertain significance33302160833021608Human1name
14706643CV631175single nucleotide variantNM_000404.4(GLB1):c.967C>G (p.Pro323Ala)GM1 gangliosidosis [RCV001175295]|Mucopolysaccharidosis, MPS-IV-B [RCV000792063]uncertain significance|not provided33304622133046221Human2name
14738330CV631176single nucleotide variantNM_000404.4(GLB1):c.827A>C (p.His276Pro)Mucopolysaccharidosis, MPS-IV-B [RCV000820882]likely pathogenic|uncertain significance33305197033051970Human1name
14728802CV631177single nucleotide variantNM_000404.4(GLB1):c.434T>C (p.Ile145Thr)Mucopolysaccharidosis, MPS-IV-B [RCV000816698]uncertain significance33306825333068253Human1name
14978001CV677122single nucleotide variantNM_000404.4(GLB1):c.545C>G (p.Thr182Arg)Infantile GM1 gangliosidosis [RCV000850228]uncertain significance33306547033065470Human1name , alternate_id
21068937CV788764single nucleotide variantNM_000404.4(GLB1):c.950G>A (p.Trp317Ter)Infantile GM1 gangliosidosis [RCV000985131]likely pathogenic33305176333051763Human1name , alternate_id
21069734CV789350single nucleotide variantNM_000404.4(GLB1):c.385G>C (p.Glu129Gln)Infantile GM1 gangliosidosis [RCV000984877]likely pathogenic33306883133068831Human1name , alternate_id
8624261CV79370single nucleotide variantNM_000404.4(GLB1):c.319T>C (p.Phe107Leu)GM1 gangliosidosis [RCV004586535]|GM1 gangliosidosis type 2 [RCV000059351]|GM1 gangliosidosis type 2 [RCV005031548]|Inborn genetic diseases [RCV000623339]|Mucopolysaccharidosis, MPS-IV-B [RCV003764741]likely pathogenic|not provided33306889733068897Human4name , alternate_id
8624262CV79371single nucleotide variantNM_000404.4(GLB1):c.518T>C (p.Leu173Pro)GM1 gangliosidosis type 2 [RCV000059352]|GM1 gangliosidosis type 2 [RCV005031549]|Mucopolysaccharidosis, MPS-IV-B [RCV000541694]pathogenic|likely pathogenic|not provided33306549733065497Human2name , alternate_id
21068512CV795400single nucleotide variantNM_000404.4(GLB1):c.921G>A (p.Met307Ile)See cases [RCV004797888]|not provided [RCV000998015]likely pathogenic|uncertain significance33305179233051792Humanname
21074787CV798530single nucleotide variantNM_000404.4(GLB1):c.716C>T (p.Thr239Met)GM1 gangliosidosis [RCV004702562]|GM1 gangliosidosis type 2 [RCV000995552]|GM1 gangliosidosis type 2 [RCV005036266]|Infantile GM1 gangliosidosis [RCV001331204]|Mucopolysaccharidosis, MPS-IV-B [RCV001378118]|not provided [RCV002279689]pathogenic|likely pathogenic33305810633058106Human4name , alternate_id
25321572CV806439single nucleotide variantNM_000404.4(GLB1):c.407C>T (p.Pro136Leu)Infantile GM1 gangliosidosis [RCV001009625]likely pathogenic33306828033068280Human1name , alternate_id
26920163CV827904single nucleotide variantNM_000404.4(GLB1):c.931G>A (p.Gly311Arg)GM1 gangliosidosis [RCV001175304]|GM1 gangliosidosis type 2 [RCV005029643]|Mucopolysaccharidosis, MPS-IV-B [RCV001059700]pathogenic|likely pathogenic|not provided33305178233051782Human3name , alternate_id
26923557CV827905single nucleotide variantNM_000404.4(GLB1):c.875C>G (p.Ser292Cys)Mucopolysaccharidosis, MPS-IV-B [RCV001064212]uncertain significance33305192233051922Human1name
40814817CV861129single nucleotide variantNM_000404.4(GLB1):c.416T>A (p.Leu139Gln)Infantile GM1 gangliosidosis [RCV001261541]likely pathogenic33306827133068271Human1name , alternate_id
28879143CV888672single nucleotide variantNM_000404.4(GLB1):c.616C>T (p.Arg206Cys)GM1 gangliosidosis [RCV001148905]|Mucopolysaccharidosis, MPS-IV-B [RCV001148904]|Mucopolysaccharidosis, MPS-IV-B [RCV002557199]uncertain significance33305820633058206Human2name
28883992CV888673single nucleotide variantNM_000404.4(GLB1):c.374A>G (p.Tyr125Cys)GM1 gangliosidosis [RCV001150421]|Mucopolysaccharidosis, MPS-IV-B [RCV001150422]uncertain significance33306884233068842Human2name
34890961CV904436single nucleotide variantNM_000404.4(GLB1):c.958G>A (p.Ala320Thr)not provided [RCV001171832]likely pathogenic|uncertain significance33304623033046230Humanname
34891810CV906358single nucleotide variantNM_000404.4(GLB1):c.574T>C (p.Tyr192His)GM1 gangliosidosis [RCV001175302]|not specified [RCV005056990]uncertain significance|not provided33305824833058248Human1name
34891802CV906362single nucleotide variantNM_000404.4(GLB1):c.380G>A (p.Cys127Tyr)GM1 gangliosidosis [RCV001175297]|Mucopolysaccharidosis, MPS-IV-B [RCV005236659]likely pathogenic|not provided33306883633068836Human2name
38468674CV920704single nucleotide variantNM_000404.4(GLB1):c.977C>T (p.Ala326Val)not provided [RCV001200665]uncertain significance33304621133046211Humanname
38468679CV920705single nucleotide variantNM_000404.4(GLB1):c.941T>G (p.Phe314Cys)not provided [RCV001200666]likely pathogenic33305177233051772Humanname
38470058CV921461single nucleotide variantNM_000404.4(GLB1):c.785G>C (p.Gly262Ala)Mucopolysaccharidosis, MPS-IV-B [RCV003770235]|not specified [RCV001201273]pathogenic|uncertain significance33305349833053498Human1name
38462480CV943476duplicationNM_000404.4(GLB1):c.1685dup (p.Asp564fs)Mucopolysaccharidosis, MPS-IV-B [RCV001232770]likely pathogenic33301410433014105Human1name
38597539CV963535single nucleotide variantNM_000404.4(GLB1):c.859G>A (p.Glu287Lys)Intellectual disability [RCV001252006]|Mucopolysaccharidosis, MPS-IV-B [RCV002570483]likely benign|uncertain significance33305193833051938Human3name
38597540CV963536single nucleotide variantNM_000404.4(GLB1):c.334C>T (p.His112Tyr)Intellectual disability [RCV001252007]likely benign33306888233068882Human2name
40888728CV971844single nucleotide variantNM_000404.4(GLB1):c.918C>A (p.Tyr306Ter)GM1 gangliosidosis type 2 [RCV001263744]likely pathogenic33305179533051795Human1name , alternate_id
40888729CV971845single nucleotide variantNM_000404.4(GLB1):c.819G>A (p.Trp273Ter)GM1 gangliosidosis type 2 [RCV001263745]|GM1 gangliosidosis type 2 [RCV005029851]|Mucopolysaccharidosis, MPS-IV-B [RCV002537662]pathogenic|likely pathogenic33305197833051978Human2name , alternate_id
40888730CV971846single nucleotide variantNM_000404.4(GLB1):c.775G>T (p.Glu259Ter)GM1 gangliosidosis type 2 [RCV001263746]likely pathogenic33305350833053508Human1name , alternate_id
8639831CV98814single nucleotide variantNM_000404.4(GLB1):c.442C>T (p.Arg148Cys)GM1 gangliosidosis [RCV000778692]|GM1 gangliosidosis type 2 [RCV000666298]|Infantile GM1 gangliosidosis [RCV001331203]|Mucopolysaccharidosis, MPS-IV-B [RCV000818014]|not provided [RCV000178094]pathogenic|likely pathogenic33306824533068245Human4name , alternate_id
8639834CV98817single nucleotide variantNM_000404.4(GLB1):c.481T>G (p.Trp161Gly)GM1 gangliosidosis [RCV001175293]|GM1 gangliosidosis type 2 [RCV000673411]|Mucopolysaccharidosis, MPS-IV-B [RCV001378119]|not provided [RCV000078717]pathogenic|likely pathogenic|uncertain significance|not provided33306553433065534Human3name , alternate_id
127267570CV1059728single nucleotide variantNM_000404.4(GLB1):c.1699C>T (p.Gln567Ter)Mucopolysaccharidosis, MPS-IV-B [RCV001389009]|not provided [RCV003481105]pathogenic|likely pathogenic33301409133014091Human1name
127271191CV1059729single nucleotide variantNM_000404.4(GLB1):c.1580G>A (p.Trp527Ter)Mucopolysaccharidosis, MPS-IV-B [RCV001390073]|Mucopolysaccharidosis, MPS-IV-B [RCV003230671]pathogenic33301421033014210Human1name
127266794CV1059730single nucleotide variantNM_000404.4(GLB1):c.1324C>T (p.Arg442Ter)GM1 gangliosidosis type 2 [RCV005023134]|Mucopolysaccharidosis, MPS-IV-B [RCV001381783]pathogenic|likely pathogenic33301847133018471Human2name , alternate_id
13782527CV543184single nucleotide variantNM_000404.4(GLB1):c.1452C>G (p.Asn484Lys)GM1 gangliosidosis type 2 [RCV000668974]|Mucopolysaccharidosis, MPS-IV-B [RCV001379670]pathogenic|likely pathogenic|conflicting interpretations of pathogenicity|uncertain significance33301673633016736Human2name , alternate_id
8555131CV106591deletionNM_000404.2:c.672_673delATInfantile GM1 gangliosidosis [RCV000087092]pathogenicHuman1alternate_id
150429572CV1189285single nucleotide variantNM_000404.4(GLB1):c.1658T>C (p.Met553Thr)GM1 gangliosidosis type 2 [RCV001563860]|GM1 gangliosidosis type 3 [RCV001563861]|Infantile GM1 gangliosidosis [RCV001563859]|Mucopolysaccharidosis, MPS-IV-B [RCV001563862]uncertain significance33301413233014132Human4alternate_id
150451096CV1200419single nucleotide variantNM_000404.4(GLB1):c.1784G>A (p.Arg595Gln)GM1 gangliosidosis type 2 [RCV001580719]|GM1 gangliosidosis type 3 [RCV001580720]|Inborn genetic diseases [RCV002573267]|Infantile GM1 gangliosidosis [RCV001580718]|Mucopolysaccharidosis, MPS-IV-B [RCV001580721]|Mucopolysaccharidosis, MPS-IV-B [RCV002573266]uncertain significance33299729532997295Human5alternate_id
150436163CV1241930single nucleotide variantNM_000404.4(GLB1):c.1010T>C (p.Leu337Pro)GM1 gangliosidosis [RCV003323912]|Infantile GM1 gangliosidosis [RCV001650518]|Mucopolysaccharidosis, MPS-IV-B [RCV001882746]pathogenic|likely pathogenic33304617833046178Human3alternate_id
150542348CV1314744microsatelliteNM_000404.4(GLB1):c.1465_1466del (p.Ile489fs)Infantile GM1 gangliosidosis [RCV001794518]likely pathogenic33301672233016723Humanalternate_id
151351351CV1323495deletionNM_000404.4(GLB1):c.425_428del (p.Lys142fs)Infantile GM1 gangliosidosis [RCV001806351]|Mucopolysaccharidosis, MPS-IV-B [RCV001869565]pathogenic33306825933068262Human2alternate_id
151351400CV1323588single nucleotide variantNM_000404.4(GLB1):c.1099C>T (p.Pro367Ser)Infantile GM1 gangliosidosis [RCV001806444]uncertain significance33302429533024295Human1alternate_id
151717644CV1495553single nucleotide variantNM_000404.4(GLB1):c.1256G>A (p.Arg419Gln)GM1 gangliosidosis type 2 [RCV002498062]|Mucopolysaccharidosis, MPS-IV-B [RCV002026850]likely pathogenic|uncertain significance33301853933018539Human2alternate_id
151711983CV1501432microsatelliteNM_000404.4(GLB1):c.435TCT[1] (p.Leu147del)GM1 gangliosidosis type 2 [RCV005025561]|Mucopolysaccharidosis, MPS-IV-B [RCV002005188]pathogenic|likely pathogenic|uncertain significance33306824733068249Humanalternate_id
8595216CV15963single nucleotide variantNM_000404.4(GLB1):c.1369C>T (p.Arg457Ter)GM1 gangliosidosis [RCV001174734]|GM1 gangliosidosis type 2 [RCV000667074]|GM1 gangliosidosis type 2 [RCV005208117]|Infantile GM1 gangliosidosis [RCV000000972]|Mucopolysaccharidosis, MPS-IV-B [RCV001058421]|not provided [RCV001781153]pathogenic33301681933016819Human4alternate_id
8595221CV15969single nucleotide variantNM_000404.4(GLB1):c.1370G>A (p.Arg457Gln)GM1 gangliosidosis [RCV002281684]|GM1 gangliosidosis type 2 [RCV001810396]|GM1 gangliosidosis type 3 [RCV000000978]|Mucopolysaccharidosis, MPS-IV-B [RCV001378633]pathogenic|likely pathogenic33301681833016818Human4alternate_id
8595223CV15971single nucleotide variantNM_000404.4(GLB1):c.1445G>A (p.Arg482His)GM1 gangliosidosis [RCV000586055]|GM1 gangliosidosis type 2 [RCV002476905]|Infantile GM1 gangliosidosis [RCV000000981]|Mucopolysaccharidosis, MPS-IV-B [RCV000119099]|Mucopolysaccharidosis, MPS-IV-B [RCV001034863]|not provided [RCV000174679]pathogenic33301674333016743Human4alternate_id
8555884CV15973duplicationNM_000404.4(GLB1):c.256_278dup (p.Gln95fs)Infantile GM1 gangliosidosis [RCV000000983]pathogenic33306893733068938Human1alternate_id
8688721CV15977single nucleotide variantNM_000404.4(GLB1):c.1444C>T (p.Arg482Cys)GM1 gangliosidosis type 2 [RCV000665872]|Mucopolysaccharidosis, MPS-IV-B [RCV000119100]|Mucopolysaccharidosis, MPS-IV-B [RCV001376852]pathogenic|likely pathogenic|uncertain significance33301674433016744Human2alternate_id
8595228CV15979single nucleotide variantNM_000404.4(GLB1):c.1313G>A (p.Gly438Glu)GM1 gangliosidosis [RCV005237344]|GM1 gangliosidosis type 2 [RCV000850556]|Mucopolysaccharidosis, MPS-IV-B [RCV000000989]|Mucopolysaccharidosis, MPS-IV-B [RCV001382999]|Spondyloepiphyseal dysplasia [RCV001843450]|not provided [RCV001091796]pathogenic33301848233018482Human5alternate_id
8595229CV15980single nucleotide variantNM_000404.4(GLB1):c.1051C>T (p.Arg351Ter)GM1 gangliosidosis type 2 [RCV000665526]|GM1-gangliosidosis, type I, with cardiac involvement [RCV000000990]|Infantile GM1 gangliosidosis [RCV001331201]|Mucopolysaccharidosis, MPS-IV-B [RCV000780302]|Mucopolysaccharidosis, MPS-IV-B [RCV001223149]|Spastic ataxia [RCV001642195]|not provided [RCV002225pathogenic|likely pathogenic33304613733046137Human5alternate_id
8595230CV15981single nucleotide variantNM_000404.4(GLB1):c.1498A>G (p.Thr500Ala)GM1 gangliosidosis [RCV002281685]|GM1 gangliosidosis type 2 [RCV000673423]|GM1 gangliosidosis type 3 [RCV003137481]|Mucopolysaccharidosis, MPS-IV-B [RCV000000991]|Mucopolysaccharidosis, MPS-IV-B [RCV001040694]|not provided [RCV001818116]pathogenic|likely pathogenic33301429233014292Human4alternate_id
8595231CV15982single nucleotide variantNM_000404.4(GLB1):c.1223A>C (p.Gln408Pro)GM1 gangliosidosis type 2 [RCV000667601]|Mucopolysaccharidosis, MPS-IV-B [RCV000000992]pathogenic|uncertain significance33302157633021576Human2alternate_id
8595235CV15987single nucleotide variantNM_000404.4(GLB1):c.1772A>G (p.Tyr591Cys)GM1 gangliosidosis type 2 [RCV000673090]|GM1 gangliosidosis type 2 [RCV005252653]|GM1-gangliosidosis, type I, with cardiac involvement [RCV000000998]|Mucopolysaccharidosis, MPS-IV-B [RCV003764505]pathogenic|likely pathogenic|uncertain significance33299730732997307Human3alternate_id
152985445CV1675146duplicationNM_000404.4(GLB1):c.1598_1601dup (p.His534fs)GM1 gangliosidosis type 2 [RCV005025734]|Mucopolysaccharidosis, MPS-IV-B [RCV002240085]pathogenic33301418833014189Human2alternate_id
9688684CV177749single nucleotide variantNM_000404.4(GLB1):c.1561T>C (p.Cys521Arg)GM1 gangliosidosis type 2 [RCV001701621]|GM1 gangliosidosis type 3 [RCV001701622]|Infantile GM1 gangliosidosis [RCV001527520]|Mucopolysaccharidosis, MPS-IV-B [RCV001521989]|Mucopolysaccharidosis, MPS-IV-B [RCV001527521]|not provided [RCV001175292]|not specified [RCV000153326]benign|not provided33301422933014229Human4alternate_id
155728284CV1782357single nucleotide variantNM_000404.4(GLB1):c.1122T>A (p.Tyr374Ter)GM1 gangliosidosis type 2 [RCV002307889]likely pathogenic33302427233024272Human1alternate_id
155729599CV1782845deletionNM_000404.4(GLB1):c.500_501del (p.Pro167fs)GM1 gangliosidosis type 2 [RCV002308377]likely pathogenic33306551433065515Human1alternate_id
155735633CV1783140deletionNM_000404.4(GLB1):c.487_488del (p.Gly163fs)GM1 gangliosidosis type 2 [RCV002309297]likely pathogenic33306552733065528Human1alternate_id
155735795CV1783239deletionNM_000404.4(GLB1):c.230_231del (p.Leu77fs)GM1 gangliosidosis type 2 [RCV002309396]likely pathogenic33307255833072559Human1alternate_id
155726671CV1783862microsatelliteNM_000404.4(GLB1):c.1379_1380del (p.Val460fs)GM1 gangliosidosis type 2 [RCV002307306]likely pathogenic33301680833016809Humanalternate_id
155737130CV1784266deletionNM_000404.4(GLB1):c.1023_1024del (p.Asp342fs)GM1 gangliosidosis type 2 [RCV002310423]likely pathogenic33304616433046165Human1alternate_id
9834717CV180917single nucleotide variantNM_058216.3(RAD51C):c.746G>A (p.Arg249His)Breast-ovarian cancer, familial, susceptibility to, 3 [RCV000663073]|Breast-ovarian cancer, familial, susceptibility to, 3 [RCV001257495]|Fanconi anemia complementation group O [RCV000168412]|Hereditary cancer-predisposing syndrome [RCV000234871]|not provided [RCV000160916]|not specified [RCV0007817likely pathogenic|conflicting interpretations of pathogenicity|uncertain significance175870989958709899Human3alternate_id
155911816CV1867771single nucleotide variantNM_000404.4(GLB1):c.1122T>G (p.Tyr374Ter)Infantile GM1 gangliosidosis [RCV002510243]pathogenic33302427233024272Human1alternate_id
155941064CV1902013single nucleotide variantNM_000404.4(GLB1):c.1147A>T (p.Lys383Ter)GM1 gangliosidosis type 2 [RCV005028217]|Mucopolysaccharidosis, MPS-IV-B [RCV003073540]pathogenic|likely pathogenic33302165233021652Human2alternate_id
10047474CV190257duplicationSingle alleleGangliosidosis GM1 type 3 [RCV000173123]|Infantile GM1 gangliosidosis [RCV000173125]|Juvenile GM>1< gangliosidosis [RCV000173124]|Mucopolysaccharidosis, MPS-IV-B [RCV000173122]pathogenicHumanalternate_id
10047873CV191495insertionNM_000404.3(GLB1):c.1466_1467insGGTGCATATAT (p.Ile489Metfs)Gangliosidosis GM1 type 3 [RCV000174676]|Infantile GM1 gangliosidosis [RCV000174678]|Juvenile GM>1< gangliosidosis [RCV000174677]|Mucopolysaccharidosis, MPS-IV-B [RCV000174675]pathogenic33301672133016722Humanalternate_id
10047950CV191759single nucleotide variantNM_000404.4(GLB1):c.1768C>T (p.Arg590Cys)GLB1-related disorder [RCV003221293]|GM1 gangliosidosis [RCV004798797]|Infantile GM1 gangliosidosis [RCV000175003]|Mucopolysaccharidosis, MPS-IV-B [RCV000703485]|Mucopolysaccharidosis, MPS-IV-B [RCV003387787]|not provided [RCV000175004]pathogenic33299731132997311Human3alternate_id
156141744CV1921940single nucleotide variantNM_000404.4(GLB1):c.2012A>G (p.Asp671Gly)GM1 gangliosidosis type 2 [RCV004725551]|Mucopolysaccharidosis, MPS-IV-B [RCV002623685]likely benign|uncertain significance33299706732997067Human2alternate_id
155912499CV1935340single nucleotide variantNM_000404.4(GLB1):c.1421A>G (p.Asp474Gly)Infantile GM1 gangliosidosis [RCV002510671]uncertain significance33301676733016767Human1alternate_id
13496518CV205010single nucleotide variantNM_000404.4(GLB1):c.1285C>T (p.Pro429Ser)GM1 gangliosidosis type 2 [RCV000673241]|Mucopolysaccharidosis, MPS-IV-B [RCV000537911]|not provided [RCV003482247]likely benign|uncertain significance33301851033018510Human2alternate_id
10409638CV211787single nucleotide variantNM_017775.3(TTC19):c.-42G>Tnot provided [RCV000196528]pathogenic171599980715999807Humanalternate_id
11531212CV247388single nucleotide variantNM_000404.4(GLB1):c.1733A>G (p.Lys578Arg)GM1 gangliosidosis [RCV001192992]|GM1 gangliosidosis type 2 [RCV000239412]|GM1 gangliosidosis type 2 [RCV000665995]|Inborn genetic diseases [RCV002518537]|Mucopolysaccharidosis, MPS-IV-B [RCV001061617]|not provided [RCV001200664]pathogenic|likely pathogenic33301405733014057Human4alternate_id
401854954CV2752690indelNM_000404.4(GLB1):c.1071_1073delinsGG (p.Phe357fs)Infantile GM1 gangliosidosis [RCV003337744]likely pathogenic33302432133024323Humanalternate_id
11598675CV294405single nucleotide variantNM_000404.4(GLB1):c.1343A>T (p.Asp448Val)GM1 gangliosidosis [RCV000292413]|GM1 gangliosidosis type 2 [RCV001775114]|GM1 gangliosidosis type 2 [RCV005027449]|Infantile GM1 gangliosidosis [RCV001584055]|Mucopolysaccharidosis, MPS-IV-B [RCV000675170]|Mucopolysaccharidosis, MPS-IV-B [RCV001382666]pathogenic|likely pathogenic|uncertain significance|not provided33301845233018452Human4alternate_id
405282058CV3224728single nucleotide variantNM_000404.4(GLB1):c.1027C>T (p.Leu343Phe)Infantile GM1 gangliosidosis [RCV003989065]uncertain significance33304616133046161Human1alternate_id
407573025CV3498802single nucleotide variantNM_000404.4(GLB1):c.1823T>C (p.Leu608Pro)GM1 gangliosidosis type 2 [RCV005023646]|Mucopolysaccharidosis, MPS-IV-B [RCV004699771]likely pathogenic33299725632997256Human2alternate_id
407573192CV3498993single nucleotide variantNM_000404.4(GLB1):c.1471G>T (p.Asp491Tyr)GM1 gangliosidosis [RCV004699962]|GM1 gangliosidosis type 2 [RCV005023649]likely pathogenic33301671733016717Human2alternate_id
408394723CV3522038microsatelliteNM_000404.4(GLB1):c.515_516del (p.Leu172fs)Infantile GM1 gangliosidosis [RCV004764831]likely pathogenic|uncertain significance33306549933065500Humanalternate_id
597638077CV3717458single nucleotide variantNM_000404.4(GLB1):c.1792C>T (p.Gln598Ter)GM1 gangliosidosis type 2 [RCV005024592]likely pathogenic33299728732997287Human1alternate_id
597638095CV3717461deletionNM_000404.4(GLB1):c.597_598del (p.Leu200fs)GM1 gangliosidosis type 2 [RCV005024595]likely pathogenic33305822433058225Human1alternate_id
597638117CV3717466indelNM_000404.4(GLB1):c.435_436delinsA (p.Leu146fs)GM1 gangliosidosis type 2 [RCV005024599]likely pathogenic33306825133068252Humanalternate_id
598212138CV4009011single nucleotide variantNM_000404.4(GLB1):c.1322A>G (p.Asp441Gly)GM1 gangliosidosis type 2 [RCV005400624]uncertain significance33301847333018473Human1alternate_id
12907195CV414933single nucleotide variantNM_000404.4(GLB1):c.1646C>T (p.Pro549Leu)Infantile GM1 gangliosidosis [RCV002286741]|Mucopolysaccharidosis, MPS-IV-B [RCV000666099]|Mucopolysaccharidosis, MPS-IV-B [RCV000811767]|not provided [RCV000490151]pathogenic|likely pathogenic33301414433014144Human2alternate_id
13483619CV443416single nucleotide variantNM_000404.4(GLB1):c.1588C>T (p.Arg530Cys)GLB1-related disorder [RCV004537876]|GM1 gangliosidosis type 2 [RCV000765726]|Mucopolysaccharidosis, MPS-IV-B [RCV001079383]|not provided [RCV000522107]likely benign|conflicting interpretations of pathogenicity|uncertain significance33301420233014202Human5alternate_id
13616424CV519256single nucleotide variantNM_000404.4(GLB1):c.1325G>A (p.Arg442Gln)GLB1-related disorder [RCV004737910]|GM1 gangliosidosis type 2 [RCV000666461]|GM1 gangliosidosis type 2 [RCV005208144]|Infantile GM1 gangliosidosis [RCV003338697]|Mucopolysaccharidosis, MPS-IV-B [RCV000633471]|not provided [RCV001568844]pathogenic|likely pathogenic33301847033018470Human5alternate_id
13790393CV542920single nucleotide variantNM_000404.4(GLB1):c.2032T>C (p.Ter678Arg)GM1 gangliosidosis type 2 [RCV000675012]uncertain significance33299704732997047Human1alternate_id
13785783CV542931single nucleotide variantNM_000404.4(GLB1):c.1714C>T (p.Gln572Ter)GM1 gangliosidosis type 2 [RCV000672277]|Mucopolysaccharidosis, MPS-IV-B [RCV002531313]pathogenic|likely pathogenic33301407633014076Human2alternate_id
13784702CV542932single nucleotide variantNM_000404.4(GLB1):c.1454A>G (p.Tyr485Cys)GM1 gangliosidosis type 2 [RCV000671173]|Mucopolysaccharidosis, MPS-IV-B [RCV001855552]|not specified [RCV004782504]pathogenic|uncertain significance33301673433016734Human2alternate_id
13790479CV542934single nucleotide variantNM_000404.4(GLB1):c.1321G>A (p.Asp441Asn)GM1 gangliosidosis type 2 [RCV000666573]|Mucopolysaccharidosis, MPS-IV-B [RCV001049111]pathogenic|likely pathogenic33301847433018474Human2alternate_id
13790406CV542958deletionNM_000404.4(GLB1):c.425_426del (p.Lys142fs)GM1 gangliosidosis type 2 [RCV000675020]likely pathogenic33306826133068262Human1alternate_id
13787889CV543091single nucleotide variantNM_000404.4(GLB1):c.2034A>C (p.Ter678Cys)GM1 gangliosidosis type 2 [RCV000673690]uncertain significance33299704532997045Human1alternate_id
13789767CV543093deletionNM_000404.4(GLB1):c.2007_2010del (p.Asn669fs)GM1 gangliosidosis type 2 [RCV000666165]uncertain significance33299706932997072Human1alternate_id
13785027CV543095single nucleotide variantNM_000404.4(GLB1):c.1978A>T (p.Arg660Ter)GM1 gangliosidosis type 2 [RCV000671539]uncertain significance33299710132997101Human1alternate_id
13790453CV543098single nucleotide variantNM_000404.4(GLB1):c.1768C>A (p.Arg590Ser)GM1 gangliosidosis type 2 [RCV000666546]|Mucopolysaccharidosis, MPS-IV-B [RCV002530688]likely pathogenic|uncertain significance33299731132997311Human2alternate_id
13787429CV543110single nucleotide variantNM_000404.4(GLB1):c.1481G>T (p.Gly494Val)GM1 gangliosidosis type 2 [RCV000664835]|Mucopolysaccharidosis, MPS-IV-B [RCV005223104]pathogenic|uncertain significance33301430933014309Human2alternate_id
13788660CV543170single nucleotide variantNM_000404.4(GLB1):c.2002A>T (p.Lys668Ter)GM1 gangliosidosis type 2 [RCV000665507]|Mucopolysaccharidosis, MPS-IV-B [RCV001868203]|not provided [RCV001771920]uncertain significance33299707732997077Human2alternate_id
13792047CV543173deletionNM_000404.4(GLB1):c.1500_1503del (p.Leu501fs)GM1 gangliosidosis type 2 [RCV000668225]likely pathogenic33301428733014290Human1alternate_id
13789310CV543186single nucleotide variantNM_000404.4(GLB1):c.1038G>T (p.Lys346Asn)GM1 gangliosidosis [RCV002271564]|GM1 gangliosidosis type 2 [RCV000674446]|Mucopolysaccharidosis, MPS-IV-B [RCV001855609]pathogenic|likely pathogenic33304615033046150Human3alternate_id
13787709CV543193single nucleotide variantNM_000404.4(GLB1):c.1783C>T (p.Arg595Trp)GM1 gangliosidosis type 2 [RCV000664993]|GM1 gangliosidosis type 2 [RCV000987138]|Inborn genetic diseases [RCV002532038]|Mucopolysaccharidosis, MPS-IV-B [RCV001868198]|See cases [RCV002252200]|not specified [RCV001797774]pathogenic|uncertain significance33299729632997296Human3alternate_id
13783253CV543194deletionNM_000404.4(GLB1):c.645_648del (p.Val216fs)GM1 gangliosidosis type 2 [RCV000669890]likely pathogenic33305817433058177Human1alternate_id
13788283CV543198single nucleotide variantNM_000404.4(GLB1):c.1746G>A (p.Trp582Ter)GM1 gangliosidosis type 2 [RCV000673883]|Mucopolysaccharidosis, MPS-IV-B [RCV001855604]|not provided [RCV003236832]pathogenic|likely pathogenic33299733332997333Human2alternate_id
13791647CV543200single nucleotide variantNM_000404.4(GLB1):c.1609G>T (p.Glu537Ter)GM1 gangliosidosis type 2 [RCV000667717]likely pathogenic33301418133014181Human1alternate_id
13784468CV543202insertionNM_000404.4(GLB1):c.1510_1511insGA (p.Asn504fs)GM1 gangliosidosis type 2 [RCV000670869]|Mucopolysaccharidosis, MPS-IV-B [RCV002531266]pathogenic|likely pathogenic33301427933014280Human2alternate_id
13789437CV543206single nucleotide variantNM_000404.4(GLB1):c.1471G>A (p.Asp491Asn)GM1 gangliosidosis type 2 [RCV000674513]|Mucopolysaccharidosis, MPS-IV-B [RCV001868281]|Mucopolysaccharidosis, MPS-IV-B [RCV002289953]pathogenic|uncertain significance33301671733016717Human2alternate_id
13782648CV543214single nucleotide variantNM_000404.4(GLB1):c.1438A>G (p.Met480Val)GM1 gangliosidosis type 2 [RCV000669124]|Mucopolysaccharidosis, MPS-IV-B [RCV004689842]|not provided [RCV003238800]likely pathogenic|conflicting interpretations of pathogenicity|uncertain significance33301675033016750Human2alternate_id
13783082CV543215single nucleotide variantNM_000404.4(GLB1):c.1310A>G (p.Asn437Ser)GLB1-related disorder [RCV004535685]|GM1 gangliosidosis [RCV001150120]|GM1 gangliosidosis type 2 [RCV000669669]|Mucopolysaccharidosis, MPS-IV-B [RCV000874342]|Mucopolysaccharidosis, MPS-IV-B [RCV001150121]|not specified [RCV002222593]benign|likely benign|uncertain significance33301848533018485Human5alternate_id
13789008CV543217single nucleotide variantNM_000404.4(GLB1):c.1038G>C (p.Lys346Asn)GM1 gangliosidosis type 2 [RCV000665726]|Mucopolysaccharidosis, MPS-IV-B [RCV000821368]pathogenic|likely pathogenic33304615033046150Human2alternate_id
13788261CV543226deletionNM_000404.4(GLB1):c.433_437del (p.Ile145fs)GM1 gangliosidosis type 2 [RCV000665277]|Mucopolysaccharidosis, MPS-IV-B [RCV002530651]pathogenic|likely pathogenic33306825033068254Human2alternate_id
13812163CV559427indelNM_000404.4(GLB1):c.817_818delinsCT (p.Trp273Leu)GM1 gangliosidosis type 2 [RCV005027848]|Infantile GM1 gangliosidosis [RCV001584562]|Mucopolysaccharidosis, MPS-IV-B [RCV000689254]|Mucopolysaccharidosis, MPS-IV-B [RCV000790561]|not provided [RCV002275106]pathogenic|likely pathogenic|not provided33305197933051980Humanalternate_id
14712083CV631174single nucleotide variantNM_000404.4(GLB1):c.1479G>T (p.Lys493Asn)Infantile GM1 gangliosidosis [RCV005208150]|Mucopolysaccharidosis, MPS-IV-B [RCV000810175]likely pathogenic|uncertain significance33301670933016709Human2alternate_id
14746712CV672002deletionNM_000404.4(GLB1):c.495_497del (p.Leu166del)GM1 gangliosidosis type 2 [RCV000844877]|Infantile GM1 gangliosidosis [RCV001585790]|Mucopolysaccharidosis, MPS-IV-B [RCV001214281]pathogenic|uncertain significance|not provided33306551833065520Human3alternate_id
25327475CV815872single nucleotide variantNM_000404.4(GLB1):c.1318C>T (p.His440Tyr)Infantile GM1 gangliosidosis [RCV001027535]pathogenic33301847733018477Human1alternate_id
26899023CV827900single nucleotide variantNM_000404.4(GLB1):c.1787G>A (p.Gly596Asp)GM1 gangliosidosis type 2 [RCV005029667]|Mucopolysaccharidosis, MPS-IV-B [RCV001070830]uncertain significance33299729232997292Human2alternate_id
26888742CV827902microsatelliteNM_000404.4(GLB1):c.1298_1299del (p.Ser433fs)GM1 gangliosidosis type 2 [RCV002307662]|Mucopolysaccharidosis, MPS-IV-B [RCV001045376]pathogenic|likely pathogenic33301849633018497Humanalternate_id
26909435CV827906deletionNM_000404.4(GLB1):c.531_534del (p.Gly178fs)GM1 gangliosidosis type 2 [RCV005029586]|Mucopolysaccharidosis, MPS-IV-B [RCV001038513]pathogenic|likely pathogenic33306548133065484Human2alternate_id
40888727CV971843single nucleotide variantNM_000404.4(GLB1):c.1312G>T (p.Gly438Ter)GM1 gangliosidosis type 2 [RCV001263743]likely pathogenic33301848333018483Human1alternate_id
8639817CV98800deletionNM_000404.4(GLB1):c.1174_1175del (p.Leu392fs)GM1 gangliosidosis type 2 [RCV000672348]|Mucopolysaccharidosis, MPS-IV-B [RCV001386115]|not provided [RCV000174243]pathogenic|likely pathogenic33302162433021625Human2alternate_id
8639819CV98802single nucleotide variantNM_000404.4(GLB1):c.1306C>T (p.Leu436Phe)GLB1-related disorder [RCV004542751]|GM1 gangliosidosis [RCV001150122]|GM1 gangliosidosis type 2 [RCV000671886]|Mucopolysaccharidosis, MPS-IV-B [RCV001150123]|Mucopolysaccharidosis, MPS-IV-B [RCV001511461]|not provided [RCV001573681]|not specified [RCV000078701]benign|likely benign|conflicting interpretations of pathogenicity|conflicting data from submitters33301848933018489Human5alternate_id
8639820CV98803single nucleotide variantNM_000404.4(GLB1):c.1310A>T (p.Asn437Ile)GM1 gangliosidosis type 2 [RCV000668735]|Mucopolysaccharidosis, MPS-IV-B [RCV001854385]|not provided [RCV000174475]pathogenic|likely pathogenic|uncertain significance33301848533018485Human2alternate_id
8639822CV98805duplicationNM_000404.4(GLB1):c.1456_1466dup (p.Ile489fs)GM1 gangliosidosis type 2 [RCV000668115]|Mucopolysaccharidosis, MPS-IV-B [RCV003764756]|not provided [RCV000174675]pathogenic|likely pathogenic33301672133016722Human2alternate_id
8639823CV98806single nucleotide variantNM_000404.4(GLB1):c.1594A>G (p.Ser532Gly)GLB1-related disorder [RCV004528281]|GM1 gangliosidosis [RCV000355730]|Infantile GM1 gangliosidosis [RCV001527519]|Mucopolysaccharidosis, MPS-IV-B [RCV000260653]|Mucopolysaccharidosis, MPS-IV-B [RCV000526685]|not provided [RCV001175303]|not specified [RCV0000787benign|likely benign|not provided33301419633014196Human3alternate_id
8639825CV98808single nucleotide variantNM_000404.4(GLB1):c.1769G>A (p.Arg590His)GM1 gangliosidosis [RCV004526614]|GM1 gangliosidosis type 2 [RCV001810420]|GM1 gangliosidosis type 2 [RCV005025132]|Infantile GM1 gangliosidosis [RCV001804833]|Mucopolysaccharidosis, MPS-IV-B [RCV000794211]|Progressive familial intrahepatic cholestasis [RCV004542752]|not provided [RCV000174999]pathogenic|likely pathogenic|uncertain significance33299731032997310Human5alternate_id
15174625CV777238single nucleotide variantNM_001286423.2(GLB1L):c.722-8T>Anot provided [RCV000950387]benign2219239841219239841Humanname
15138834CV779691single nucleotide variantNM_001370461.1(GLB1L2):c.1708-6T>Gnot provided [RCV000965860]likely benign11134374596134374596Humanname
8652798CV129373single nucleotide variantNM_001080407.2(GLB1L3):c.637-1792A>GLung cancer [RCV000109860]uncertain significance11134287006134287006Humanname
153347388CV1692036microsatelliteNM_000404.4(GLB1):c.955+142_955+143insTTTTCTnot provided [RCV002273521]likely benign33305161533051616Humanname
150339123CV1167291microsatelliteNM_000404.4(GLB1):c.955+142_955+143insTTTTCTTTTnot provided [RCV001534063]benign33305161533051616Humanname
12893527CV406181indelNM_000404.4(GLB1):c.902_914+17delinsAGGCAAGTATATACTTGCCnot provided [RCV000479288]likely pathogenic33305186633051895Humanname
156193502CV2066484indelNM_000404.4(GLB1):c.914+15_914+16delinsAGTGTGAACTTGTGAGTGTTTMucopolysaccharidosis, MPS-IV-B [RCV002828689]uncertain significance33305186733051868Humanname
155794450CV1858574insertionNM_000404.4(GLB1):c.1068+2341_1068+2342insGCTTGGTATTTTTTCTGAGGGTATCTTTGCTTGGTATTTTTCTGAGTTAGCTTTTGCTTGTATTTTTTTTTCTGATGTACTTTSchizophrenia [RCV002463536]uncertain significance33304377833043779Human2name