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


More than 1000 records found for search term Hgs (Displaying 1000)
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
15158840CV760673single nucleotide variantNM_004712.5(HGS):c.416-9T>Cnot provided [RCV000925159]likely benign178169017381690173Humanname
15185707CV778426single nucleotide variantNM_004712.5(HGS):c.199-9C>Tnot provided [RCV000953062]benign178168699481686994Humanname
15149690CV731192single nucleotide variantNM_004712.5(HGS):c.1567-7C>Tnot provided [RCV000879219]benign178169660081696600Humanname
15168838CV745115single nucleotide variantNM_004712.5(HGS):c.1567-6G>Anot provided [RCV000904940]likely benign178169660181696601Humanname
15119483CV715828single nucleotide variantNM_004712.5(HGS):c.891G>T (p.Ser297=)not provided [RCV000962558]benign178169392081693920Humanname
156331719CV2218207single nucleotide variantNM_004712.5(HGS):c.238C>T (p.His80Tyr)not specified [RCV004088411]uncertain significance178168704281687042Humanname
401888012CV2781837single nucleotide variantNM_004712.5(HGS):c.161A>C (p.Asn54Thr)not specified [RCV004356789]uncertain significance178168635081686350Humanname
401907924CV2818098single nucleotide variantNM_004712.5(HGS):c.1221G>A (p.Gln407=)not provided [RCV003422979]likely benign178169582781695827Humanname
401907926CV2818099single nucleotide variantNM_004712.5(HGS):c.1446G>A (p.Gly482=)not provided [RCV003422980]likely benign178169640981696409Humanname
405777113CV3270065single nucleotide variantNM_004712.5(HGS):c.251C>G (p.Ala84Gly)not specified [RCV004396982]uncertain significance178168705581687055Humanname
15099333CV704470single nucleotide variantNM_004712.5(HGS):c.1998T>A (p.Thr666=)not provided [RCV000958746]benign178170058281700582Humanname
15178256CV741209single nucleotide variantNM_004712.5(HGS):c.1374C>T (p.Asn458=)not provided [RCV000906836]benign178169598081695980Humanname
15144130CV756288single nucleotide variantNM_004712.5(HGS):c.1974C>T (p.Pro658=)not provided [RCV000922314]likely benign178170055881700558Humanname
156118117CV2346012single nucleotide variantNM_004712.5(HGS):c.748C>G (p.Pro250Ala)not specified [RCV004201493]uncertain significance178169366081693660Humanname
401745132CV2693187single nucleotide variantNM_004712.5(HGS):c.709T>C (p.Tyr237His)not specified [RCV004293118]uncertain significance178169354981693549Humanname
401870717CV2766290single nucleotide variantNM_004712.5(HGS):c.851C>T (p.Ser284Phe)not specified [RCV004342546]uncertain significance178169388081693880Humanname
401864215CV2767550single nucleotide variantNM_004712.5(HGS):c.698T>G (p.Leu233Arg)not specified [RCV004343703]uncertain significance178169353881693538Humanname
401891486CV2769178single nucleotide variantNM_004712.5(HGS):c.304G>T (p.Val102Leu)not specified [RCV004349021]uncertain significance178168871681688716Humanname
401906631CV2818097single nucleotide variantNM_004712.5(HGS):c.538C>T (p.His180Tyr)not provided [RCV003421555]uncertain significance178169144781691447Humanname
405777122CV3270066single nucleotide variantNM_004712.5(HGS):c.364G>A (p.Glu122Lys)not specified [RCV004396983]uncertain significance178168877681688776Humanname
405777131CV3270067single nucleotide variantNM_004712.5(HGS):c.713T>C (p.Leu238Pro)not specified [RCV004396984]uncertain significance178169355381693553Humanname
405777137CV3270068single nucleotide variantNM_004712.5(HGS):c.720C>A (p.Ser240Arg)not specified [RCV004396985]uncertain significance178169356081693560Humanname
405777143CV3270069single nucleotide variantNM_004712.5(HGS):c.724C>A (p.Leu242Met)not specified [RCV004396986]uncertain significance178169356481693564Humanname
405777149CV3270070single nucleotide variantNM_004712.5(HGS):c.731A>C (p.Gln244Pro)not specified [RCV004396987]uncertain significance178169357181693571Humanname
405777162CV3270072single nucleotide variantNM_004712.5(HGS):c.734A>C (p.Gln245Pro)not specified [RCV004396989]uncertain significance178169357481693574Humanname
405777168CV3270073single nucleotide variantNM_004712.5(HGS):c.887C>T (p.Pro296Leu)not specified [RCV004396990]uncertain significance178169391681693916Humanname
405777174CV3270074single nucleotide variantNM_004712.5(HGS):c.947C>T (p.Ala316Val)not specified [RCV004396991]uncertain significance178169482581694825Humanname
597761514CV3685732single nucleotide variantNM_004712.5(HGS):c.706G>A (p.Glu236Lys)not specified [RCV004925923]uncertain significance178169354681693546Humanname
597761533CV3685736single nucleotide variantNM_004712.5(HGS):c.944C>T (p.Ser315Leu)not specified [RCV004925927]uncertain significance178169482281694822Humanname
597761544CV3685739single nucleotide variantNM_004712.5(HGS):c.314G>A (p.Arg105His)not specified [RCV004925930]uncertain significance178168872681688726Humanname
597761559CV3685742single nucleotide variantNM_004712.5(HGS):c.340G>A (p.Ala114Thr)not specified [RCV004925933]uncertain significance178168875281688752Humanname
597761562CV3685743single nucleotide variantNM_004712.5(HGS):c.764C>T (p.Thr255Met)not specified [RCV004925934]uncertain significance178169367681693676Humanname
597761565CV3685744single nucleotide variantNM_004712.5(HGS):c.430G>C (p.Glu144Gln)not specified [RCV004925935]uncertain significance178169019681690196Humanname
597761580CV3685748single nucleotide variantNM_004712.5(HGS):c.503G>A (p.Arg168His)not specified [RCV004925938]uncertain significance178169070881690708Humanname
598177435CV3978735single nucleotide variantNM_004712.5(HGS):c.701C>G (p.Pro234Arg)not specified [RCV005351833]uncertain significance178169354181693541Humanname
598177441CV3978736single nucleotide variantNM_004712.5(HGS):c.709T>G (p.Tyr237Asp)not specified [RCV005351834]uncertain significance178169354981693549Humanname
598177452CV3978739single nucleotide variantNM_004712.5(HGS):c.733C>G (p.Gln245Glu)not specified [RCV005351836]uncertain significance178169357381693573Humanname
15142762CV741208single nucleotide variantNM_004712.5(HGS):c.739C>G (p.Gln247Glu)not provided [RCV000899727]likely benign178169357981693579Humanname
156372738CV2194576single nucleotide variantNM_004712.5(HGS):c.2297C>A (p.Ala766Glu)not specified [RCV004081634]uncertain significance178170158181701581Humanname
156251427CV2212334single nucleotide variantNM_004712.5(HGS):c.2276C>T (p.Pro759Leu)not specified [RCV004091282]uncertain significance178170156081701560Humanname
155932951CV2228771single nucleotide variantNM_004712.5(HGS):c.1163G>A (p.Gly388Asp)not specified [RCV004093238]uncertain significance178169520781695207Humanname
155986053CV2233952single nucleotide variantNM_004712.5(HGS):c.1910A>G (p.Tyr637Cys)not specified [RCV004104295]uncertain significance178170049481700494Humanname
155943046CV2244884single nucleotide variantNM_004712.5(HGS):c.1909T>A (p.Tyr637Asn)not specified [RCV004104638]uncertain significance178170049381700493Humanname
156093072CV2256721single nucleotide variantNM_004712.5(HGS):c.1789G>A (p.Gly597Ser)not specified [RCV004118892]uncertain significance178169690581696905Humanname
156313957CV2257087single nucleotide variantNM_004712.5(HGS):c.2191T>A (p.Tyr731Asn)not specified [RCV004123052]uncertain significance178170109981701099Humanname
156034915CV2282938single nucleotide variantNM_004712.5(HGS):c.1475G>A (p.Arg492Gln)not specified [RCV004143577]uncertain significance178169643881696438Humanname
156085212CV2289787single nucleotide variantNM_004712.5(HGS):c.1282A>G (p.Met428Val)not specified [RCV004150468]likely benign178169588881695888Humanname
156012752CV2291295single nucleotide variantNM_004712.5(HGS):c.1819G>A (p.Val607Met)not specified [RCV004153572]uncertain significance178169693581696935Humanname
156087018CV2299082single nucleotide variantNM_004712.5(HGS):c.1729G>A (p.Gly577Arg)not specified [RCV004152445]uncertain significance178169684581696845Humanname
155905910CV2303206single nucleotide variantNM_004712.5(HGS):c.2020G>A (p.Val674Met)not specified [RCV004156965]uncertain significance178170069881700698Humanname
156035344CV2303433single nucleotide variantNM_004712.5(HGS):c.1331A>G (p.Gln444Arg)not specified [RCV004159768]uncertain significance178169593781695937Humanname
156198889CV2312953single nucleotide variantNM_004712.5(HGS):c.1730G>T (p.Gly577Val)not specified [RCV004159461]uncertain significance178169684681696846Humanname
155905068CV2385676single nucleotide variantNM_004712.5(HGS):c.2198C>T (p.Ala733Val)not specified [RCV004233304]uncertain significance178170110681701106Humanname
155903884CV2386643single nucleotide variantNM_004712.5(HGS):c.1028G>A (p.Arg343His)not specified [RCV004230984]uncertain significance178169497681694976Humanname
329383098CV2465528single nucleotide variantNM_004712.5(HGS):c.1909T>C (p.Tyr637His)not specified [RCV004281277]uncertain significance178170049381700493Humanname
401753154CV2674796single nucleotide variantNM_004712.5(HGS):c.1142C>G (p.Ser381Cys)not specified [RCV004294075]uncertain significance178169518681695186Humanname
401733694CV2682611single nucleotide variantNM_004712.5(HGS):c.2192A>C (p.Tyr731Ser)not specified [RCV004292662]uncertain significance178170110081701100Humanname
401721076CV2702255single nucleotide variantNM_004712.5(HGS):c.1006G>A (p.Glu336Lys)not specified [RCV004314590]uncertain significance178169495481694954Humanname
401859129CV2771396single nucleotide variantNM_004712.5(HGS):c.1919G>T (p.Gly640Val)not specified [RCV004348453]uncertain significance178170050381700503Humanname
405777108CV3270064single nucleotide variantNM_004712.5(HGS):c.1346T>C (p.Met449Thr)not specified [RCV004396981]uncertain significance178169595281695952Humanname
407522087CV3437242single nucleotide variantNM_004712.5(HGS):c.2291C>T (p.Pro764Leu)not specified [RCV004630551]uncertain significance178170157581701575Humanname
407521910CV3437243single nucleotide variantNM_004712.5(HGS):c.1108A>G (p.Asn370Asp)not specified [RCV004630552]uncertain significance178169505681695056Humanname
407521913CV3437244single nucleotide variantNM_004712.5(HGS):c.1243G>A (p.Ala415Thr)not specified [RCV004630553]uncertain significance178169584981695849Humanname
407510653CV3437247single nucleotide variantNM_004712.5(HGS):c.1040C>T (p.Thr347Met)not specified [RCV004626192]uncertain significance178169498881694988Humanname
407521923CV3437248single nucleotide variantNM_004712.5(HGS):c.1751C>T (p.Ser584Leu)not specified [RCV004630556]uncertain significance178169686781696867Humanname
597761509CV3685731single nucleotide variantNM_004712.5(HGS):c.1759G>T (p.Ala587Ser)not specified [RCV004925922]uncertain significance178169687581696875Humanname
597761519CV3685733single nucleotide variantNM_004712.5(HGS):c.1810A>G (p.Met604Val)not specified [RCV004925924]uncertain significance178169692681696926Humanname
597761524CV3685734single nucleotide variantNM_004712.5(HGS):c.1928G>T (p.Gly643Val)not specified [RCV004925925]uncertain significance178170051281700512Humanname
597761528CV3685735single nucleotide variantNM_004712.5(HGS):c.1474C>T (p.Arg492Trp)not specified [RCV004925926]uncertain significance178169643781696437Humanname
597761538CV3685737single nucleotide variantNM_004712.5(HGS):c.1961C>T (p.Pro654Leu)not specified [RCV004925928]uncertain significance178170054581700545Humanname
597761540CV3685738single nucleotide variantNM_004712.5(HGS):c.1502A>T (p.Glu501Val)not specified [RCV004925929]uncertain significance178169646581696465Humanname
597761549CV3685740single nucleotide variantNM_004712.5(HGS):c.1180C>T (p.Pro394Ser)not specified [RCV004925931]uncertain significance178169578681695786Humanname
597761554CV3685741single nucleotide variantNM_004712.5(HGS):c.2158A>G (p.Ser720Gly)not specified [RCV004925932]likely benign178170106681701066Humanname
597761570CV3685746single nucleotide variantNM_004712.5(HGS):c.1730G>C (p.Gly577Ala)not specified [RCV004925936]uncertain significance178169684681696846Humanname
597761575CV3685747single nucleotide variantNM_004712.5(HGS):c.1825A>C (p.Met609Leu)not specified [RCV004925937]uncertain significance178169694181696941Humanname
598177408CV3978729single nucleotide variantNM_004712.5(HGS):c.1258G>A (p.Val420Met)not specified [RCV005351828]uncertain significance178169586481695864Humanname
598177414CV3978730single nucleotide variantNM_004712.5(HGS):c.1163G>T (p.Gly388Val)not specified [RCV005351829]uncertain significance178169520781695207Humanname
598177419CV3978731single nucleotide variantNM_004712.5(HGS):c.1433G>A (p.Arg478His)not specified [RCV005351830]uncertain significance178169639681696396Humanname
598177430CV3978734single nucleotide variantNM_004712.5(HGS):c.1432C>T (p.Arg478Cys)not specified [RCV005351832]uncertain significance178169639581696395Humanname
598247885CV3978737single nucleotide variantNM_004712.5(HGS):c.1931C>T (p.Ala644Val)not specified [RCV005345365]uncertain significance178170051581700515Humanname
598177447CV3978738single nucleotide variantNM_004712.5(HGS):c.1709T>A (p.Leu570His)not specified [RCV005351835]uncertain significance178169682581696825Humanname
15103347CV704468single nucleotide variantNM_004712.5(HGS):c.1200G>C (p.Glu400Asp)not provided [RCV000959461]benign178169580681695806Humanname
15194029CV704469single nucleotide variantNM_004712.5(HGS):c.1891A>G (p.Met631Val)not provided [RCV000955534]likely benign178170047581700475Humanname
405273209CV3210346single nucleotide variantNM_152419.3(HGSNAT):c.*8C>THGSNAT-related disorder [RCV003914572]likely benign84319957743199577Humanname , trait , alternate_id
28867957CV899645single nucleotide variantNM_152419.3(HGSNAT):c.-3G>CMucopolysaccharidosis, MPS-III-C [RCV001162198]uncertain significance84314049443140494Human1name
11653872CV314503single nucleotide variantNM_152419.2(HGSNAT):c.-37C>TSanfilippo syndrome [RCV000313800]uncertain significance84314046043140460Human1name
11605604CV305411single nucleotide variantNM_152419.3(HGSNAT):c.*585T>CMucopolysaccharidosis, MPS-III-C [RCV000321329]benign|likely benign84320015443200154Human1name
11608578CV309258single nucleotide variantNM_152419.3(HGSNAT):c.*149G>TMucopolysaccharidosis, MPS-III-C [RCV000357005]uncertain significance84319971843199718Human1name
11644364CV309274single nucleotide variantNM_152419.3(HGSNAT):c.*160C>TMucopolysaccharidosis, MPS-III-C [RCV000259828]uncertain significance84319972943199729Human1name
11599827CV314531single nucleotide variantNM_152419.3(HGSNAT):c.*390G>AMucopolysaccharidosis, MPS-III-C [RCV000268623]|not provided [RCV004696075]uncertain significance84319995943199959Human1name
11651437CV314602single nucleotide variantNM_152419.3(HGSNAT):c.*196T>GMucopolysaccharidosis, MPS-III-C [RCV000299141]uncertain significance84319976543199765Human1name
11608872CV314603single nucleotide variantNM_152419.3(HGSNAT):c.*304C>AMucopolysaccharidosis, MPS-III-C [RCV000360941]uncertain significance84319987343199873Human1name
14725731CV663356single nucleotide variantNM_152419.2(HGSNAT):c.-174G>Anot provided [RCV000833565]benign84314032343140323Humanname
28872308CV899658single nucleotide variantNM_152419.3(HGSNAT):c.*106G>AMucopolysaccharidosis, MPS-III-C [RCV001164336]likely benign84319967543199675Human1name
28907246CV899659single nucleotide variantNM_152419.3(HGSNAT):c.*477G>AMucopolysaccharidosis, MPS-III-C [RCV001159411]benign84320004643200046Human1name
28907248CV899660single nucleotide variantNM_152419.3(HGSNAT):c.*574C>GMucopolysaccharidosis, MPS-III-C [RCV001159412]uncertain significance84320014343200143Human1name
28907250CV899661single nucleotide variantNM_152419.3(HGSNAT):c.*581T>CMucopolysaccharidosis, MPS-III-C [RCV001159413]uncertain significance84320015043200150Human1name
28907252CV899662single nucleotide variantNM_152419.3(HGSNAT):c.*600C>TMucopolysaccharidosis, MPS-III-C [RCV001159414]benign84320016943200169Human1name
28907254CV899663single nucleotide variantNM_152419.3(HGSNAT):c.*612A>CMucopolysaccharidosis, MPS-III-C [RCV001159415]uncertain significance84320018143200181Human1name
28907256CV899664single nucleotide variantNM_152419.3(HGSNAT):c.*619T>CMucopolysaccharidosis, MPS-III-C [RCV001159416]uncertain significance84320018843200188Human1name
28907258CV899665single nucleotide variantNM_152419.3(HGSNAT):c.*649A>GMucopolysaccharidosis, MPS-III-C [RCV001159417]uncertain significance84320021843200218Human1name
28909660CV899666single nucleotide variantNM_152419.3(HGSNAT):c.*733G>TMucopolysaccharidosis, MPS-III-C [RCV001160785]benign84320030243200302Human1name
28909663CV899667single nucleotide variantNM_152419.3(HGSNAT):c.*772C>GMucopolysaccharidosis, MPS-III-C [RCV001160786]uncertain significance84320034143200341Human1name
28909666CV899668single nucleotide variantNM_152419.3(HGSNAT):c.*778T>CMucopolysaccharidosis, MPS-III-C [RCV001160787]uncertain significance84320034743200347Human1name
28909669CV899669single nucleotide variantNM_152419.3(HGSNAT):c.*817C>TMucopolysaccharidosis, MPS-III-C [RCV001160788]|not provided [RCV004707566]likely benign84320038643200386Human1name
28909671CV899670single nucleotide variantNM_152419.3(HGSNAT):c.*851A>GMucopolysaccharidosis, MPS-III-C [RCV001160789]uncertain significance84320042043200420Human1name
28909674CV899671single nucleotide variantNM_152419.3(HGSNAT):c.*857C>TMucopolysaccharidosis, MPS-III-C [RCV001160790]uncertain significance84320042643200426Human1name
28909677CV899672single nucleotide variantNM_152419.3(HGSNAT):c.*871C>AMucopolysaccharidosis, MPS-III-C [RCV001160791]uncertain significance84320044043200440Human1name
127256191CV1055732single nucleotide variantNM_152419.3(HGSNAT):c.563+2T>AMucopolysaccharidosis, MPS-III-C [RCV001379518]likely pathogenic84316150943161509Human1name
127280944CV1075398single nucleotide variantNM_152419.3(HGSNAT):c.494-4C>AMucopolysaccharidosis, MPS-III-C [RCV001410132]likely benign84316143443161434Human1name
127272035CV1075400single nucleotide variantNM_152419.3(HGSNAT):c.563+7T>CMucopolysaccharidosis, MPS-III-C [RCV001405571]likely benign84316151443161514Human1name
127252342CV1075401single nucleotide variantNM_152419.3(HGSNAT):c.563+8A>GMucopolysaccharidosis, MPS-III-C [RCV001418055]likely benign84316151543161515Human1name
127252814CV1075402single nucleotide variantNM_152419.3(HGSNAT):c.564-8A>GMucopolysaccharidosis, MPS-III-C [RCV001418158]likely benign84316916543169165Human1name
127281697CV1075405single nucleotide variantNM_152419.3(HGSNAT):c.743+7G>AMucopolysaccharidosis, MPS-III-C [RCV001410644]likely benign84317070143170701Human1name
127245301CV1075407single nucleotide variantNM_152419.3(HGSNAT):c.852-7T>GMucopolysaccharidosis, MPS-III-C [RCV001398701]likely benign84317806743178067Human1name
127255664CV1097073single nucleotide variantNM_152419.3(HGSNAT):c.634-8T>AMucopolysaccharidosis, MPS-III-C [RCV001437500]likely benign84317057743170577Human1name
127276690CV1097076single nucleotide variantNM_152419.3(HGSNAT):c.851+9C>TMucopolysaccharidosis, MPS-III-C [RCV001432928]likely benign84317375243173752Human1name
127324917CV1118621single nucleotide variantNM_152419.3(HGSNAT):c.372-8G>AMucopolysaccharidosis, MPS-III-C [RCV001468311]likely benign84315891543158915Human1name
127324846CV1118625single nucleotide variantNM_152419.3(HGSNAT):c.821-9G>TMucopolysaccharidosis, MPS-III-C [RCV001468293]likely benign84317370443173704Human1name
127326934CV1139496single nucleotide variantNM_152419.3(HGSNAT):c.118+8C>GMucopolysaccharidosis, MPS-III-C [RCV001506436]likely benign84314062243140622Human1name
127310048CV1155970duplicationNM_152419.3(HGSNAT):c.564-4dupMucopolysaccharidosis, MPS-III-C [RCV001518121]benign84316916543169166Human1name
150447261CV1274415single nucleotide variantNM_152419.3(HGSNAT):c.493+5G>AMucopolysaccharidosis, MPS-III-C [RCV002538631]|Retinitis pigmentosa 73 [RCV003323916]|not provided [RCV001699670]likely pathogenic|uncertain significance84315904943159049Human2name
151809183CV1338660single nucleotide variantNM_152419.3(HGSNAT):c.743+4T>CMucopolysaccharidosis, MPS-III-C [RCV002012266]uncertain significance84317069843170698Human1name
151821178CV1388878single nucleotide variantNM_152419.3(HGSNAT):c.493+4C>TMucopolysaccharidosis, MPS-III-C [RCV001975744]|Retinal dystrophy [RCV004816858]uncertain significance84315904843159048Human3name
151887608CV1472031single nucleotide variantNM_152419.3(HGSNAT):c.118+2T>CMucopolysaccharidosis, MPS-III-C [RCV002000919]likely pathogenic84314061643140616Human1name
151728481CV1515730single nucleotide variantNM_152419.3(HGSNAT):c.118+1G>AMucopolysaccharidosis, MPS-III-C [RCV001983953]likely pathogenic84314061543140615Human1name
152051556CV1528020single nucleotide variantNM_152419.3(HGSNAT):c.235-4A>GMucopolysaccharidosis, MPS-III-C [RCV002089224]likely benign84315857143158571Human1name
152161172CV1531022single nucleotide variantNM_152419.3(HGSNAT):c.633+9T>CMucopolysaccharidosis, MPS-III-C [RCV002123220]likely benign84316925143169251Human1name
152096116CV1559781single nucleotide variantNM_152419.3(HGSNAT):c.118+8C>TMucopolysaccharidosis, MPS-III-C [RCV002213379]likely benign84314062243140622Human1name
152045080CV1590642single nucleotide variantNM_152419.3(HGSNAT):c.851+7T>GMucopolysaccharidosis, MPS-III-C [RCV002108248]likely benign84317375043173750Human1name
152101478CV1606885single nucleotide variantNM_152419.3(HGSNAT):c.119-9T>CMucopolysaccharidosis, MPS-III-C [RCV002195605]likely benign84314693943146939Human1name
152149348CV1616784single nucleotide variantNM_152419.3(HGSNAT):c.371+9C>TMucopolysaccharidosis, MPS-III-C [RCV002201727]likely benign84315872043158720Human1name
152070322CV1622819single nucleotide variantNM_152419.3(HGSNAT):c.119-5A>GMucopolysaccharidosis, MPS-III-C [RCV002209892]likely benign84314694343146943Human1name
8595349CV16269single nucleotide variantNM_152419.3(HGSNAT):c.493+1G>AInborn genetic diseases [RCV002512639]|Mucopolysaccharidosis, MPS-III-C [RCV000001289]|Mucopolysaccharidosis, MPS-III-C [RCV000763183]|Sanfilippo syndrome [RCV000780343]|not provided [RCV005414443]pathogenic84315904543159045Human3name
8595354CV16275single nucleotide variantNM_152419.3(HGSNAT):c.372-2A>GMucopolysaccharidosis, MPS-III-C [RCV000001295]|Mucopolysaccharidosis, MPS-III-C [RCV001067306]|Sanfilippo syndrome [RCV000586364]|not provided [RCV005429210]pathogenic84315892143158921Human2name
152031615CV1629196single nucleotide variantNM_152419.3(HGSNAT):c.564-4T>GMucopolysaccharidosis, MPS-III-C [RCV002106200]likely benign84316916943169169Human1name
152176486CV1631423single nucleotide variantNM_152419.3(HGSNAT):c.821-4G>TMucopolysaccharidosis, MPS-III-C [RCV002164631]likely benign84317370943173709Human1name
152157925CV1639463single nucleotide variantNM_152419.3(HGSNAT):c.118+7G>AMucopolysaccharidosis, MPS-III-C [RCV002180404]likely benign84314062143140621Human1name
152057543CV1651832single nucleotide variantNM_152419.3(HGSNAT):c.744-4C>GMucopolysaccharidosis, MPS-III-C [RCV002190143]likely benign84317230643172306Human1name
152147918CV1653814single nucleotide variantNM_152419.3(HGSNAT):c.371+8C>TMucopolysaccharidosis, MPS-III-C [RCV002139081]likely benign84315871943158719Human1name
152170271CV1663200single nucleotide variantNM_152419.3(HGSNAT):c.821-9G>AMucopolysaccharidosis, MPS-III-C [RCV002183095]likely benign84317370443173704Human1name
156353805CV1880013single nucleotide variantNM_152419.3(HGSNAT):c.820+6A>GMucopolysaccharidosis, MPS-III-C [RCV003065076]uncertain significance84317239243172392Human1name
156441863CV1941516single nucleotide variantNM_152419.3(HGSNAT):c.494-1G>AMucopolysaccharidosis, MPS-III-C [RCV003112196]pathogenic84316143743161437Human1name
155944537CV2003087single nucleotide variantNM_152419.3(HGSNAT):c.744-2A>CMucopolysaccharidosis, MPS-III-C [RCV002685668]likely pathogenic84317230843172308Human1name
156134452CV2047986single nucleotide variantNM_152419.3(HGSNAT):c.234+5G>AMucopolysaccharidosis, MPS-III-C [RCV002800733]uncertain significance84314706843147068Human1name
155936651CV2058055single nucleotide variantNM_152419.3(HGSNAT):c.634-2A>GMucopolysaccharidosis, MPS-III-C [RCV002815418]likely pathogenic84317058343170583Human1name
155927229CV2070900single nucleotide variantNM_152419.3(HGSNAT):c.563+1G>CMucopolysaccharidosis, MPS-III-C [RCV002838585]likely pathogenic84316150843161508Human1name
156105872CV2089057single nucleotide variantNM_152419.3(HGSNAT):c.494-2A>GMucopolysaccharidosis, MPS-III-C [RCV002848255]pathogenic|likely pathogenic84316143643161436Human1name
156126266CV2100550single nucleotide variantNM_152419.3(HGSNAT):c.494-8T>AMucopolysaccharidosis, MPS-III-C [RCV002889764]likely benign84316143043161430Human1name
156100603CV2107349single nucleotide variantNM_152419.3(HGSNAT):c.493+4C>GMucopolysaccharidosis, MPS-III-C [RCV002927037]|not specified [RCV005059079]uncertain significance84315904843159048Human1name
156033245CV2152710single nucleotide variantNM_152419.3(HGSNAT):c.118+9A>CMucopolysaccharidosis, MPS-III-C [RCV003018764]likely benign84314062343140623Human1name
156324464CV2163308single nucleotide variantNM_152419.3(HGSNAT):c.564-1G>AMucopolysaccharidosis, MPS-III-C [RCV003029396]likely pathogenic84316917243169172Human1name
156335352CV2168338single nucleotide variantNM_152419.3(HGSNAT):c.563+9T>CMucopolysaccharidosis, MPS-III-C [RCV003029992]likely benign84316151643161516Human1name
11610430CV305416single nucleotide variantNM_152419.3(HGSNAT):c.*1137C>TMucopolysaccharidosis, MPS-III-C [RCV000381686]uncertain significance84320070643200706Human1name
11611876CV305417single nucleotide variantNM_152419.3(HGSNAT):c.*1251C>AMucopolysaccharidosis, MPS-III-C [RCV000400470]uncertain significance84320082043200820Human1name
11656691CV305418single nucleotide variantNM_152419.3(HGSNAT):c.*1378C>TMucopolysaccharidosis, MPS-III-C [RCV000335655]uncertain significance84320094743200947Human1name
11611208CV305420single nucleotide variantNM_152419.3(HGSNAT):c.*1801T>CMucopolysaccharidosis, MPS-III-C [RCV000391978]|not provided [RCV004712593]benign84320137043201370Human1name
11605113CV305421single nucleotide variantNM_152419.3(HGSNAT):c.*2643G>AMucopolysaccharidosis, MPS-III-C [RCV000315957]uncertain significance84320221243202212Human1name
405024311CV3082019single nucleotide variantNM_152419.3(HGSNAT):c.821-9G>CMucopolysaccharidosis, MPS-III-C [RCV003785625]likely benign84317370443173704Human1name
11646595CV309279single nucleotide variantNM_152419.3(HGSNAT):c.*1064A>GMucopolysaccharidosis, MPS-III-C [RCV000271912]uncertain significance84320063343200633Human1name
11602879CV309289single nucleotide variantNM_152419.3(HGSNAT):c.*1204C>AMucopolysaccharidosis, MPS-III-C [RCV000294628]uncertain significance84320077343200773Human1name
11600930CV309290single nucleotide variantNM_152419.3(HGSNAT):c.*1331T>AMucopolysaccharidosis, MPS-III-C [RCV000278297]uncertain significance84320090043200900Human1name
11652486CV309301single nucleotide variantNM_152419.3(HGSNAT):c.*1750C>TMucopolysaccharidosis, MPS-III-C [RCV000305431]uncertain significance84320131943201319Human1name
11608622CV309302single nucleotide variantNM_152419.3(HGSNAT):c.*1780C>TMucopolysaccharidosis, MPS-III-C [RCV000357878]|not provided [RCV004712592]benign|likely benign84320134943201349Human1name
11601114CV309314single nucleotide variantNM_152419.3(HGSNAT):c.*2502A>GMucopolysaccharidosis, MPS-III-C [RCV000279544]uncertain significance84320207143202071Human1name
404984233CV3096433single nucleotide variantNM_152419.3(HGSNAT):c.820+7T>CMucopolysaccharidosis, MPS-III-C [RCV003791982]likely benign84317239343172393Human1name
404988752CV3097116single nucleotide variantNM_152419.3(HGSNAT):c.372-9T>CMucopolysaccharidosis, MPS-III-C [RCV003792505]likely benign84315891443158914Human1name
405029134CV3098221single nucleotide variantNM_152419.3(HGSNAT):c.118+7G>CMucopolysaccharidosis, MPS-III-C [RCV003806514]likely benign84314062143140621Human1name
405032064CV3098627single nucleotide variantNM_152419.3(HGSNAT):c.744-6T>CMucopolysaccharidosis, MPS-III-C [RCV003806751]likely benign84317230443172304Human1name
405096251CV3105701single nucleotide variantNM_152419.3(HGSNAT):c.852-8C>GMucopolysaccharidosis, MPS-III-C [RCV003801418]likely benign84317806643178066Human1name
405008964CV3109023single nucleotide variantNM_152419.3(HGSNAT):c.493+1G>CMucopolysaccharidosis, MPS-III-C [RCV003804690]pathogenic84315904543159045Human1name
405111180CV3110762deletionNM_152419.3(HGSNAT):c.821-5delMucopolysaccharidosis, MPS-III-C [RCV003813665]likely benign84317370843173708Human1name
405127412CV3112054single nucleotide variantNM_152419.3(HGSNAT):c.820+1G>AMucopolysaccharidosis, MPS-III-C [RCV003815528]likely pathogenic84317238743172387Human1name
405128182CV3112141single nucleotide variantNM_152419.3(HGSNAT):c.371+5G>TMucopolysaccharidosis, MPS-III-C [RCV003815615]uncertain significance84315871643158716Human1name
405106870CV3113685single nucleotide variantNM_152419.3(HGSNAT):c.372-4G>TMucopolysaccharidosis, MPS-III-C [RCV003812807]likely benign84315891943158919Human1name
405080405CV3114809single nucleotide variantNM_152419.3(HGSNAT):c.852-2A>GMucopolysaccharidosis, MPS-III-C [RCV003810372]pathogenic84317807243178072Human1name
11606573CV314533single nucleotide variantNM_152419.3(HGSNAT):c.*1212C>TMucopolysaccharidosis, MPS-III-C [RCV000333217]benign|likely benign84320078143200781Human1name
11602752CV314535single nucleotide variantNM_152419.3(HGSNAT):c.*1216G>AMucopolysaccharidosis, MPS-III-C [RCV000293369]|not provided [RCV004712590]benign|likely benign84320078543200785Human1name
11606882CV314536single nucleotide variantNM_152419.3(HGSNAT):c.*1231G>AMucopolysaccharidosis, MPS-III-C [RCV000336841]|not provided [RCV004712591]benign|likely benign84320080043200800Human1name
11611759CV314537single nucleotide variantNM_152419.3(HGSNAT):c.*1436A>GMucopolysaccharidosis, MPS-III-C [RCV000399558]uncertain significance84320100543201005Human1name
11652935CV314539single nucleotide variantNM_152419.3(HGSNAT):c.*1841G>AMucopolysaccharidosis, MPS-III-C [RCV000308131]uncertain significance84320141043201410Human1name
11609467CV314542single nucleotide variantNM_152419.3(HGSNAT):c.*2258A>GMucopolysaccharidosis, MPS-III-C [RCV000368442]likely benign|uncertain significance84320182743201827Human1name
11600448CV314548single nucleotide variantNM_152419.3(HGSNAT):c.*2266G>TMucopolysaccharidosis, MPS-III-C [RCV000273779]uncertain significance84320183543201835Human1name
11610957CV314554single nucleotide variantNM_152419.3(HGSNAT):c.*2341G>AMucopolysaccharidosis, MPS-III-C [RCV000388118]uncertain significance84320191043201910Human1name
11648215CV314555single nucleotide variantNM_152419.3(HGSNAT):c.*2801C>GMucopolysaccharidosis, MPS-III-C [RCV000280853]uncertain significance84320237043202370Human1name
11657274CV314556duplicationNM_152419.3(HGSNAT):c.*3044dupSanfilippo syndrome [RCV000340219]uncertain significance84320260443202605Human1name
11649240CV314558single nucleotide variantNM_152419.3(HGSNAT):c.*3241A>GMucopolysaccharidosis, MPS-III-C [RCV000286284]uncertain significance84320281043202810Human1name
11661588CV314605single nucleotide variantNM_152419.3(HGSNAT):c.*1034G>AMucopolysaccharidosis, MPS-III-C [RCV000378131]uncertain significance84320060343200603Human1name
11610701CV314606single nucleotide variantNM_152419.3(HGSNAT):c.*1215C>TMucopolysaccharidosis, MPS-III-C [RCV000385352]uncertain significance84320078443200784Human1name
11609000CV314610single nucleotide variantNM_152419.3(HGSNAT):c.*1854C>TMucopolysaccharidosis, MPS-III-C [RCV000362781]uncertain significance84320142343201423Human1name
11600286CV314611single nucleotide variantNM_152419.3(HGSNAT):c.*2068A>GMucopolysaccharidosis, MPS-III-C [RCV000272755]uncertain significance84320163743201637Human1name
11606147CV314612single nucleotide variantNM_152419.3(HGSNAT):c.*2233G>AMucopolysaccharidosis, MPS-III-C [RCV000327885]uncertain significance84320180243201802Human1name
11656435CV314614single nucleotide variantNM_152419.3(HGSNAT):c.*2305A>GMucopolysaccharidosis, MPS-III-C [RCV000333664]uncertain significance84320187443201874Human1name
11609966CV314623single nucleotide variantNM_152419.3(HGSNAT):c.*2756G>AMucopolysaccharidosis, MPS-III-C [RCV000375262]uncertain significance84320232543202325Human1name
11611066CV314625single nucleotide variantNM_152419.3(HGSNAT):c.*3213T>AMucopolysaccharidosis, MPS-III-C [RCV000390163]|not provided [RCV004705467]likely benign|uncertain significance84320278243202782Human1name
597652469CV3722781single nucleotide variantNM_152419.3(HGSNAT):c.119-2A>CMucopolysaccharidosis, MPS-III-C [RCV005041221]likely pathogenic84314694643146946Human1name
597870105CV3866248single nucleotide variantNM_152419.3(HGSNAT):c.372-7T>CMucopolysaccharidosis, MPS-III-C [RCV005215589]likely benign84315891643158916Human1name
597851376CV3873385single nucleotide variantNM_152419.3(HGSNAT):c.494-7T>CMucopolysaccharidosis, MPS-III-C [RCV005212828]likely benign84316143143161431Human1name
597930527CV3879333single nucleotide variantNM_152419.3(HGSNAT):c.371+5G>AMucopolysaccharidosis, MPS-III-C [RCV005224830]uncertain significance84315871643158716Human1name
598123027CV3884665deletionNM_152419.3(HGSNAT):c.-5_-4delnot specified [RCV005238271]uncertain significance84314049143140492Humanname
8602335CV39789single nucleotide variantNM_152419.3(HGSNAT):c.234+1G>AMucopolysaccharidosis, MPS-III-C [RCV000023817]|Mucopolysaccharidosis, MPS-III-C [RCV000652843]|Retinal dystrophy [RCV001074236]|Sanfilippo syndrome [RCV001192638]|not provided [RCV000153361]pathogenic84314706443147064Human4name
13521231CV495386single nucleotide variantNM_152419.3(HGSNAT):c.852-2A>CMucopolysaccharidosis, MPS-III-C [RCV000669939]|Mucopolysaccharidosis, MPS-III-C [RCV001041537]|not provided [RCV000599289]pathogenic|likely pathogenic84317807243178072Human1name
13704748CV539012single nucleotide variantNM_152419.3(HGSNAT):c.235-9T>GMucopolysaccharidosis, MPS-III-C [RCV000661918]|Mucopolysaccharidosis, MPS-III-C [RCV001470454]|Retinitis pigmentosa 73 [RCV000661919]likely benign|uncertain significance84315856643158566Human2name
13789616CV544421deletionNM_152419.3(HGSNAT):c.743+1delMucopolysaccharidosis, MPS-III-C [RCV000674597]likely pathogenic84317069143170691Human1name
13791489CV544734single nucleotide variantNM_152419.3(HGSNAT):c.851+1G>AMucopolysaccharidosis, MPS-III-C [RCV000667514]likely pathogenic84317374443173744Human1name
13784449CV544774single nucleotide variantNM_152419.3(HGSNAT):c.744-2A>GMucopolysaccharidosis, MPS-III-C [RCV000670844]pathogenic|likely pathogenic84317230843172308Human1name
13786051CV544779single nucleotide variantNM_152419.3(HGSNAT):c.852-1G>AMucopolysaccharidosis, MPS-III-C [RCV000672518]|Mucopolysaccharidosis, MPS-III-C [RCV001383039]pathogenic84317807343178073Human1name
13787086CV544826single nucleotide variantNM_152419.3(HGSNAT):c.851+1G>TMucopolysaccharidosis, MPS-III-C [RCV000673270]likely pathogenic84317374443173744Human1name
15105581CV787737single nucleotide variantNM_152419.3(HGSNAT):c.234+8T>AMucopolysaccharidosis, MPS-III-C [RCV000976464]likely benign84314707143147071Human1name
26909577CV857232single nucleotide variantNM_152419.3(HGSNAT):c.118+5G>AMucopolysaccharidosis, MPS-III-C [RCV002557896]|Retinal dystrophy [RCV001073674]likely pathogenic|uncertain significance84314061943140619Human3name
28909679CV899673single nucleotide variantNM_152419.3(HGSNAT):c.*1026G>CMucopolysaccharidosis, MPS-III-C [RCV001160792]uncertain significance84320059543200595Human1name
28868301CV899674single nucleotide variantNM_152419.3(HGSNAT):c.*1086G>CMucopolysaccharidosis, MPS-III-C [RCV001162406]benign84320065543200655Human1name
28868303CV899675single nucleotide variantNM_152419.3(HGSNAT):c.*1112C>TMucopolysaccharidosis, MPS-III-C [RCV001162407]uncertain significance84320068143200681Human1name
28868305CV899676single nucleotide variantNM_152419.3(HGSNAT):c.*1214C>AMucopolysaccharidosis, MPS-III-C [RCV001162408]uncertain significance84320078343200783Human1name
28872563CV899677single nucleotide variantNM_152419.3(HGSNAT):c.*1219G>AMucopolysaccharidosis, MPS-III-C [RCV001164456]uncertain significance84320078843200788Human1name
28907423CV899678single nucleotide variantNM_152419.3(HGSNAT):c.*1584A>GMucopolysaccharidosis, MPS-III-C [RCV001159522]uncertain significance84320115343201153Human1name
28907426CV899679single nucleotide variantNM_152419.3(HGSNAT):c.*1696T>GMucopolysaccharidosis, MPS-III-C [RCV001159523]uncertain significance84320126543201265Human1name
28909819CV899680single nucleotide variantNM_152419.3(HGSNAT):c.*1925A>GMucopolysaccharidosis, MPS-III-C [RCV001160902]uncertain significance84320149443201494Human1name
28909821CV899681single nucleotide variantNM_152419.3(HGSNAT):c.*1942A>GMucopolysaccharidosis, MPS-III-C [RCV001160903]benign84320151143201511Human1name
28868465CV899682single nucleotide variantNM_152419.3(HGSNAT):c.*2434G>AMucopolysaccharidosis, MPS-III-C [RCV001162510]uncertain significance84320200343202003Human1name
28868468CV899683single nucleotide variantNM_152419.3(HGSNAT):c.*2472G>CMucopolysaccharidosis, MPS-III-C [RCV001162511]uncertain significance84320204143202041Human1name
28868470CV899684single nucleotide variantNM_152419.3(HGSNAT):c.*2538A>GMucopolysaccharidosis, MPS-III-C [RCV001162512]uncertain significance84320210743202107Human1name
28868473CV899685single nucleotide variantNM_152419.3(HGSNAT):c.*2591G>AMucopolysaccharidosis, MPS-III-C [RCV001162513]uncertain significance84320216043202160Human1name
28868474CV899686single nucleotide variantNM_152419.3(HGSNAT):c.*2620A>CMucopolysaccharidosis, MPS-III-C [RCV001162514]uncertain significance84320218943202189Human1name
28868476CV899687single nucleotide variantNM_152419.3(HGSNAT):c.*2740C>TMucopolysaccharidosis, MPS-III-C [RCV001162515]likely benign84320230943202309Human1name
28872740CV899688single nucleotide variantNM_152419.3(HGSNAT):c.*2755C>TMucopolysaccharidosis, MPS-III-C [RCV001164549]benign84320232443202324Human1name
28872744CV899689single nucleotide variantNM_152419.3(HGSNAT):c.*2767C>TMucopolysaccharidosis, MPS-III-C [RCV001164550]likely benign84320233643202336Human1name
28872745CV899690single nucleotide variantNM_152419.3(HGSNAT):c.*2802C>GMucopolysaccharidosis, MPS-III-C [RCV001164551]likely benign84320237143202371Human1name
28872747CV899691single nucleotide variantNM_152419.3(HGSNAT):c.*2806G>CMucopolysaccharidosis, MPS-III-C [RCV001164552]uncertain significance84320237543202375Human1name
28872751CV899692single nucleotide variantNM_152419.3(HGSNAT):c.*2950A>GMucopolysaccharidosis, MPS-III-C [RCV001164553]uncertain significance84320251943202519Human1name
28872753CV899693single nucleotide variantNM_152419.3(HGSNAT):c.*2967C>TMucopolysaccharidosis, MPS-III-C [RCV001164554]uncertain significance84320253643202536Human1name
28907593CV899694single nucleotide variantNM_152419.3(HGSNAT):c.*3086C>TMucopolysaccharidosis, MPS-III-C [RCV001159633]uncertain significance84320265543202655Human1name
28907595CV899695single nucleotide variantNM_152419.3(HGSNAT):c.*3176G>AMucopolysaccharidosis, MPS-III-C [RCV001159634]uncertain significance84320274543202745Human1name
28907598CV899696single nucleotide variantNM_152419.3(HGSNAT):c.*3198G>AMucopolysaccharidosis, MPS-III-C [RCV001159635]uncertain significance84320276743202767Human1name
28872066CV900502single nucleotide variantNM_152419.3(HGSNAT):c.563+3A>GMucopolysaccharidosis, MPS-III-C [RCV001164229]uncertain significance84316151043161510Human1name
8643411CV102394single nucleotide variantNM_152419.3(HGSNAT):c.1250+1G>AMucopolysaccharidosis, MPS-III-C [RCV000668206]|Mucopolysaccharidosis, MPS-III-C [RCV001065437]|Retinal dystrophy [RCV001074721]|Retinitis pigmentosa 73 [RCV002288581]|Sanfilippo syndrome [RCV001192639]|not provided [RCV000082652]pathogenic|likely pathogenic84319159643191596Human5name
8643413CV102396single nucleotide variantNM_152419.3(HGSNAT):c.1464+1G>AMucopolysaccharidosis, MPS-III-C [RCV000671662]|Mucopolysaccharidosis, MPS-III-C [RCV001221115]|not provided [RCV000082654]pathogenic|likely pathogenic84319384443193844Human1name
127278626CV1075406single nucleotide variantNM_152419.3(HGSNAT):c.744-10C>AMucopolysaccharidosis, MPS-III-C [RCV001408563]likely benign84317230043172300Human1name
127273900CV1075411single nucleotide variantNM_152419.3(HGSNAT):c.1377+7G>CMucopolysaccharidosis, MPS-III-C [RCV001406190]likely benign84319243743192437Human1name
127233368CV1075414single nucleotide variantNM_152419.3(HGSNAT):c.1464+9T>AMucopolysaccharidosis, MPS-III-C [RCV001413844]likely benign84319385243193852Human1name
127231183CV1075416single nucleotide variantNM_152419.3(HGSNAT):c.1613+8T>CMucopolysaccharidosis, MPS-III-C [RCV001412937]likely benign84319775043197750Human1name
127264154CV1097064single nucleotide variantNM_152419.3(HGSNAT):c.118+10C>AMucopolysaccharidosis, MPS-III-C [RCV001439558]likely benign84314062443140624Human1name
127264439CV1097078single nucleotide variantNM_152419.3(HGSNAT):c.1129-7C>TMucopolysaccharidosis, MPS-III-C [RCV001439634]likely benign84319146743191467Human1name
127261526CV1097086single nucleotide variantNM_152419.3(HGSNAT):c.1465-5T>CMucopolysaccharidosis, MPS-III-C [RCV001428076]likely benign84319694343196943Human1name
127281040CV1097087single nucleotide variantNM_152419.3(HGSNAT):c.1614-6T>CMucopolysaccharidosis, MPS-III-C [RCV001446861]likely benign84319783443197834Human1name
127302219CV1118629single nucleotide variantNM_152419.3(HGSNAT):c.1013-4G>AMucopolysaccharidosis, MPS-III-C [RCV001461571]likely benign84318214143182141Human1name
127334029CV1118635single nucleotide variantNM_152419.3(HGSNAT):c.1543-7A>GMucopolysaccharidosis, MPS-III-C [RCV001473327]likely benign84319766543197665Human1name
127331840CV1139500single nucleotide variantNM_152419.3(HGSNAT):c.564-10T>AMucopolysaccharidosis, MPS-III-C [RCV001489088]likely benign84316916343169163Human1name
127326412CV1139501single nucleotide variantNM_152419.3(HGSNAT):c.633+20G>CMucopolysaccharidosis, MPS-III-C [RCV001506287]likely benign84316926243169262Human1name
127307266CV1155969single nucleotide variantNM_152419.3(HGSNAT):c.493+13T>AMucopolysaccharidosis, MPS-III-C [RCV001517023]benign84315905743159057Human1name
150337687CV1166525single nucleotide variantNM_152419.3(HGSNAT):c.371+82C>TMucopolysaccharidosis, MPS-III-C [RCV001532798]|Retinitis pigmentosa 73 [RCV001532799]|not provided [RCV001676030]benign84315879343158793Human2name
150411000CV1190781single nucleotide variantNM_152419.3(HGSNAT):c.118+32G>Cnot provided [RCV001566340]likely benign84314064643140646Humanname
150439610CV1221330single nucleotide variantNM_152419.3(HGSNAT):c.235-75G>Anot provided [RCV001610025]benign84315850043158500Humanname
150431558CV1235486single nucleotide variantNM_152419.3(HGSNAT):c.563+50C>Tnot provided [RCV001641856]benign84316155743161557Humanname
150442051CV1246829single nucleotide variantNM_152419.3(HGSNAT):c.118+54C>Tnot provided [RCV001666483]benign84314066843140668Humanname
150511933CV1284820deletionNM_152419.3(HGSNAT):c.119-23delnot provided [RCV001721689]benign84314691043146910Humanname
150544439CV1313343single nucleotide variantNM_152419.3(HGSNAT):c.1542+2T>Cnot provided [RCV001783420]pathogenic84319702743197027Humanname
151790607CV1397283single nucleotide variantNM_152419.3(HGSNAT):c.1250+6C>TMucopolysaccharidosis, MPS-III-C [RCV001952011]uncertain significance84319160143191601Human1name
151841564CV1428739deletionNM_152419.3(HGSNAT):c.1464+1delMucopolysaccharidosis, MPS-III-C [RCV001994815]pathogenic84319384343193843Human1name
151889534CV1436035single nucleotide variantNM_152419.3(HGSNAT):c.1129-7C>AMucopolysaccharidosis, MPS-III-C [RCV001963448]likely benign|uncertain significance84319146743191467Human1name
151798691CV1503960single nucleotide variantNM_152419.3(HGSNAT):c.1378-2A>GMucopolysaccharidosis, MPS-III-C [RCV001973705]likely pathogenic84319375543193755Human1name
151770897CV1514800single nucleotide variantNM_152419.3(HGSNAT):c.1543-2A>GMucopolysaccharidosis, MPS-III-C [RCV002045234]|Retinitis pigmentosa 73 [RCV005254012]pathogenic|likely pathogenic84319767043197670Human2name
152051293CV1521381single nucleotide variantNM_152419.3(HGSNAT):c.118+10C>TMucopolysaccharidosis, MPS-III-C [RCV002145723]likely benign84314062443140624Human1name
152098006CV1534427single nucleotide variantNM_152419.3(HGSNAT):c.494-15C>AMucopolysaccharidosis, MPS-III-C [RCV002095121]likely benign84316142343161423Human1name
152169760CV1538698single nucleotide variantNM_152419.3(HGSNAT):c.1377+9G>CMucopolysaccharidosis, MPS-III-C [RCV002182913]likely benign84319243943192439Human1name
152173521CV1539572single nucleotide variantNM_152419.3(HGSNAT):c.743+10C>TMucopolysaccharidosis, MPS-III-C [RCV002162838]likely benign84317070443170704Human1name
152116049CV1540911single nucleotide variantNM_152419.3(HGSNAT):c.118+20C>GMucopolysaccharidosis, MPS-III-C [RCV002197409]likely benign84314063443140634Human1name
152036156CV1545935single nucleotide variantNM_152419.3(HGSNAT):c.743+17G>AMucopolysaccharidosis, MPS-III-C [RCV002164973]likely benign84317071143170711Human1name
152032655CV1546369single nucleotide variantNM_152419.3(HGSNAT):c.821-28T>CMucopolysaccharidosis, MPS-III-C [RCV002124789]benign84317368543173685Human1name
152120018CV1547317single nucleotide variantNM_152419.3(HGSNAT):c.821-30T>CMucopolysaccharidosis, MPS-III-C [RCV002081424]likely benign84317368343173683Human1name
152115659CV1553856single nucleotide variantNM_152419.3(HGSNAT):c.235-13C>GMucopolysaccharidosis, MPS-III-C [RCV002117151]likely benign84315856243158562Human1name
152045925CV1556185single nucleotide variantNM_152419.3(HGSNAT):c.821-27T>GMucopolysaccharidosis, MPS-III-C [RCV002206920]likely benign84317368643173686Human1name
152074202CV1557447single nucleotide variantNM_152419.3(HGSNAT):c.1013-9C>GMucopolysaccharidosis, MPS-III-C [RCV002129997]likely benign84318213643182136Human1name
152074387CV1557556single nucleotide variantNM_152419.3(HGSNAT):c.494-12C>TMucopolysaccharidosis, MPS-III-C [RCV002130021]likely benign84316142643161426Human1name
152057153CV1567241single nucleotide variantNM_152419.3(HGSNAT):c.851+14C>GMucopolysaccharidosis, MPS-III-C [RCV002146368]likely benign84317375743173757Human1name
152074083CV1570371deletionNM_152419.3(HGSNAT):c.1012+8delMucopolysaccharidosis, MPS-III-C [RCV002210361]likely benign84317824243178242Human1name
152171898CV1575654single nucleotide variantNM_152419.3(HGSNAT):c.118+20C>TMucopolysaccharidosis, MPS-III-C [RCV002183658]likely benign84314063443140634Human1name
152120493CV1576206single nucleotide variantNM_152419.3(HGSNAT):c.1465-7C>TMucopolysaccharidosis, MPS-III-C [RCV002197983]likely benign84319694143196941Human1name
152175852CV1580097single nucleotide variantNM_152419.3(HGSNAT):c.852-13A>GMucopolysaccharidosis, MPS-III-C [RCV002163989]likely benign84317806143178061Human1name
152159491CV1588103single nucleotide variantNM_152419.3(HGSNAT):c.1377+7G>AMucopolysaccharidosis, MPS-III-C [RCV002180679]likely benign84319243743192437Human1name
152087084CV1589917single nucleotide variantNM_152419.3(HGSNAT):c.118+12C>GMucopolysaccharidosis, MPS-III-C [RCV002193772]likely benign84314062643140626Human1name
152153932CV1592954single nucleotide variantNM_152419.3(HGSNAT):c.118+17T>CMucopolysaccharidosis, MPS-III-C [RCV002202405]likely benign84314063143140631Human1name
152162305CV1608827single nucleotide variantNM_152419.3(HGSNAT):c.851+10C>GMucopolysaccharidosis, MPS-III-C [RCV002104029]likely benign84317375343173753Human1name
152165115CV1611271single nucleotide variantNM_152419.3(HGSNAT):c.1251-6T>CMucopolysaccharidosis, MPS-III-C [RCV002141656]likely benign84319229843192298Human1name
152165714CV1611425single nucleotide variantNM_152419.3(HGSNAT):c.1129-6A>GMucopolysaccharidosis, MPS-III-C [RCV002141772]likely benign84319146843191468Human1name
152062107CV1612387single nucleotide variantNM_152419.3(HGSNAT):c.1614-9C>TMucopolysaccharidosis, MPS-III-C [RCV002168121]likely benign84319783143197831Human1name
152127108CV1615081single nucleotide variantNM_152419.3(HGSNAT):c.118+16C>GMucopolysaccharidosis, MPS-III-C [RCV002082363]likely benign84314063043140630Human1name
152073139CV1615364single nucleotide variantNM_152419.3(HGSNAT):c.234+17A>GMucopolysaccharidosis, MPS-III-C [RCV002091865]likely benign84314708043147080Human1name
152159198CV1621084single nucleotide variantNM_152419.3(HGSNAT):c.1250+7G>CMucopolysaccharidosis, MPS-III-C [RCV002203140]likely benign84319160243191602Human1name
152115387CV1628213single nucleotide variantNM_152419.3(HGSNAT):c.851+16G>TMucopolysaccharidosis, MPS-III-C [RCV002197328]likely benign84317375943173759Human1name
152035732CV1635976single nucleotide variantNM_152419.3(HGSNAT):c.1465-9C>TMucopolysaccharidosis, MPS-III-C [RCV002106944]likely benign84319693943196939Human1name
152111425CV1640391single nucleotide variantNM_152419.3(HGSNAT):c.234+18C>TMucopolysaccharidosis, MPS-III-C [RCV002174383]likely benign84314708143147081Human1name
152075058CV1652878single nucleotide variantNM_152419.3(HGSNAT):c.234+10A>TMucopolysaccharidosis, MPS-III-C [RCV002148590]likely benign84314707343147073Human1name
152090773CV1654907single nucleotide variantNM_152419.3(HGSNAT):c.851+19C>TMucopolysaccharidosis, MPS-III-C [RCV002212693]likely benign84317376243173762Human1name
152067427CV1660100single nucleotide variantNM_152419.3(HGSNAT):c.563+20C>TMucopolysaccharidosis, MPS-III-C [RCV002147619]likely benign84316152743161527Human1name
155267629CV1705029single nucleotide variantNM_152419.3(HGSNAT):c.118+69C>Tnot provided [RCV002285634]likely benign84314068343140683Humanname
155948982CV1869297single nucleotide variantNM_152419.3(HGSNAT):c.1012+7A>GMucopolysaccharidosis, MPS-III-C [RCV003074032]likely benign84317824143178241Human1name
155944568CV1875214single nucleotide variantNM_152419.3(HGSNAT):c.1613+5G>AMucopolysaccharidosis, MPS-III-C [RCV003073764]uncertain significance84319774743197747Human1name
156354920CV1880164single nucleotide variantNM_152419.3(HGSNAT):c.744-16T>CMucopolysaccharidosis, MPS-III-C [RCV003065156]likely benign|uncertain significance84317229443172294Human1name
155976916CV1886110single nucleotide variantNM_152419.3(HGSNAT):c.119-12A>GMucopolysaccharidosis, MPS-III-C [RCV003075462]likely benign84314693643146936Human1name
156401599CV1889156single nucleotide variantNM_152419.3(HGSNAT):c.851+19C>AMucopolysaccharidosis, MPS-III-C [RCV003069193]likely benign84317376243173762Human1name
156411495CV1893248single nucleotide variantNM_152419.3(HGSNAT):c.118+18A>GMucopolysaccharidosis, MPS-III-C [RCV003072503]likely benign84314063243140632Human1name
156416918CV1908761single nucleotide variantNM_152419.3(HGSNAT):c.1465-6C>TMucopolysaccharidosis, MPS-III-C [RCV002610428]likely benign84319694243196942Human1name
156444103CV1937625single nucleotide variantNM_152419.3(HGSNAT):c.1727-3A>CMucopolysaccharidosis, MPS-III-C [RCV003115022]uncertain significance84319938543199385Human1name
156449146CV1944406duplicationNM_152419.3(HGSNAT):c.1012+7dupMucopolysaccharidosis, MPS-III-C [RCV003121258]likely benign84317824043178241Human1name
156449147CV1944407single nucleotide variantNM_152419.3(HGSNAT):c.1012+8C>AMucopolysaccharidosis, MPS-III-C [RCV003121259]likely benign84317824243178242Human1name
156221010CV1965335single nucleotide variantNM_152419.3(HGSNAT):c.634-18C>GMucopolysaccharidosis, MPS-III-C [RCV002596459]likely benign84317056743170567Human1name
156075631CV1979189single nucleotide variantNM_152419.3(HGSNAT):c.118+13C>GMucopolysaccharidosis, MPS-III-C [RCV002621379]likely benign84314062743140627Human1name
156122225CV1998338single nucleotide variantNM_152419.3(HGSNAT):c.1614-5C>TMucopolysaccharidosis, MPS-III-C [RCV002662900]likely benign84319783543197835Human1name
156285942CV2001711single nucleotide variantNM_152419.3(HGSNAT):c.744-19C>GMucopolysaccharidosis, MPS-III-C [RCV002647008]likely benign84317229143172291Human1name
156362515CV2003302single nucleotide variantNM_152419.3(HGSNAT):c.821-14T>CMucopolysaccharidosis, MPS-III-C [RCV002676339]likely benign84317369943173699Human1name
156012404CV2008917single nucleotide variantNM_152419.3(HGSNAT):c.493+16C>GMucopolysaccharidosis, MPS-III-C [RCV002690586]likely benign84315906043159060Human1name
155957891CV2040255single nucleotide variantNM_152419.3(HGSNAT):c.821-31C>TMucopolysaccharidosis, MPS-III-C [RCV002776113]likely benign84317368243173682Human1name
156054311CV2060186single nucleotide variantNM_152419.3(HGSNAT):c.633+10G>AMucopolysaccharidosis, MPS-III-C [RCV002796871]likely benign84316925243169252Human1name
156328595CV2064993single nucleotide variantNM_152419.3(HGSNAT):c.820+19G>CMucopolysaccharidosis, MPS-III-C [RCV002835161]likely benign84317240543172405Human1name
156229852CV2093752single nucleotide variantNM_152419.3(HGSNAT):c.494-13T>CMucopolysaccharidosis, MPS-III-C [RCV002894510]likely benign84316142543161425Human1name
156015719CV2114392single nucleotide variantNM_152419.3(HGSNAT):c.1614-1G>CMucopolysaccharidosis, MPS-III-C [RCV002909353]likely pathogenic84319783943197839Human1name
155944418CV2143201single nucleotide variantNM_152419.3(HGSNAT):c.851+11G>AMucopolysaccharidosis, MPS-III-C [RCV002994259]likely benign84317375443173754Human1name
156000194CV2149354single nucleotide variantNM_152419.3(HGSNAT):c.118+16C>TMucopolysaccharidosis, MPS-III-C [RCV002996981]likely benign84314063043140630Human1name
156177592CV2166444single nucleotide variantNM_152419.3(HGSNAT):c.1251-9C>TMucopolysaccharidosis, MPS-III-C [RCV003023725]likely benign84319229543192295Human1name
156003549CV2166517single nucleotide variantNM_152419.3(HGSNAT):c.372-11A>TMucopolysaccharidosis, MPS-III-C [RCV003017389]likely benign84315891243158912Human1name
156327778CV2184531single nucleotide variantNM_152419.3(HGSNAT):c.1251-4C>GMucopolysaccharidosis, MPS-III-C [RCV003047032]likely benign84319230043192300Human1name
156258221CV2264937single nucleotide variantNM_152419.3(HGSNAT):c.1614-2A>GInborn genetic diseases [RCV002831542]uncertain significance84319783843197838Human1name
11544884CV253146single nucleotide variantNM_152419.3(HGSNAT):c.493+46G>Tnot provided [RCV001545448]|not specified [RCV000244390]benign|likely benign84315909043159090Humanname
329952027CV2668770single nucleotide variantNM_152419.3(HGSNAT):c.1250+5G>Anot specified [RCV003230851]uncertain significance84319160043191600Humanname
11599114CV305403single nucleotide variantNM_152419.3(HGSNAT):c.234+14C>GMucopolysaccharidosis, MPS-III-C [RCV000263117]|Mucopolysaccharidosis, MPS-III-C [RCV001514319]|not provided [RCV000514120]benign|likely benign|uncertain significance84314707743147077Human1name
405052342CV3084771single nucleotide variantNM_152419.3(HGSNAT):c.634-20T>GMucopolysaccharidosis, MPS-III-C [RCV003798178]likely benign84317056543170565Human1name
404997915CV3085762single nucleotide variantNM_152419.3(HGSNAT):c.494-16T>CMucopolysaccharidosis, MPS-III-C [RCV003783132]likely benign84316142243161422Human1name
402521049CV3086317single nucleotide variantNM_152419.3(HGSNAT):c.1726+1G>AMucopolysaccharidosis, MPS-III-C [RCV003781090]likely pathogenic84319795343197953Human1name
402521680CV3086548single nucleotide variantNM_152419.3(HGSNAT):c.563+18G>AMucopolysaccharidosis, MPS-III-C [RCV003781164]likely benign84316152543161525Human1name
405020055CV3087976single nucleotide variantNM_152419.3(HGSNAT):c.118+11A>GMucopolysaccharidosis, MPS-III-C [RCV003795536]likely benign84314062543140625Human1name
402503847CV3090120single nucleotide variantNM_152419.3(HGSNAT):c.851+17C>TMucopolysaccharidosis, MPS-III-C [RCV003788887]likely benign84317376043173760Human1name
402486436CV3090406single nucleotide variantNM_152419.3(HGSNAT):c.821-26G>AMucopolysaccharidosis, MPS-III-C [RCV003787066]likely benign84317368743173687Human1name
402486449CV3090407single nucleotide variantNM_152419.3(HGSNAT):c.235-18T>CMucopolysaccharidosis, MPS-III-C [RCV003787067]likely benign84315855743158557Human1name
402489347CV3090895single nucleotide variantNM_152419.3(HGSNAT):c.634-16C>TMucopolysaccharidosis, MPS-III-C [RCV003787397]likely benign84317056943170569Human1name
402517969CV3091771single nucleotide variantNM_152419.3(HGSNAT):c.493+14C>GMucopolysaccharidosis, MPS-III-C [RCV003790217]likely benign84315905843159058Human1name
405035728CV3093180single nucleotide variantNM_152419.3(HGSNAT):c.851+16G>CMucopolysaccharidosis, MPS-III-C [RCV003786531]likely benign84317375943173759Human1name
405012084CV3093437single nucleotide variantNM_152419.3(HGSNAT):c.118+11A>CMucopolysaccharidosis, MPS-III-C [RCV003784441]likely benign84314062543140625Human1name
405028336CV3094869single nucleotide variantNM_152419.3(HGSNAT):c.851+19C>GMucopolysaccharidosis, MPS-III-C [RCV003796231]likely benign84317376243173762Human1name
405029941CV3095180single nucleotide variantNM_152419.3(HGSNAT):c.633+19A>GMucopolysaccharidosis, MPS-III-C [RCV003796385]likely benign84316926143169261Human1name
405001581CV3095506single nucleotide variantNM_152419.3(HGSNAT):c.1727-9C>TMucopolysaccharidosis, MPS-III-C [RCV003793809]likely benign84319937943199379Human1name
405003619CV3095698single nucleotide variantNM_152419.3(HGSNAT):c.493+14C>TMucopolysaccharidosis, MPS-III-C [RCV003794003]likely benign84315905843159058Human1name
405009865CV3096576single nucleotide variantNM_152419.3(HGSNAT):c.744-20T>GMucopolysaccharidosis, MPS-III-C [RCV003794565]likely benign84317229043172290Human1name
405010299CV3096618single nucleotide variantNM_152419.3(HGSNAT):c.234+20C>TMucopolysaccharidosis, MPS-III-C [RCV003794607]likely benign84314708343147083Human1name
404978782CV3099107single nucleotide variantNM_152419.3(HGSNAT):c.234+10A>CMucopolysaccharidosis, MPS-III-C [RCV003791087]likely benign84314707343147073Human1name
404978864CV3099123single nucleotide variantNM_152419.3(HGSNAT):c.744-15G>TMucopolysaccharidosis, MPS-III-C [RCV003791104]likely benign84317229543172295Human1name
404979038CV3099323single nucleotide variantNM_152419.3(HGSNAT):c.118+13C>TMucopolysaccharidosis, MPS-III-C [RCV003791151]likely benign84314062743140627Human1name
404980949CV3099678single nucleotide variantNM_152419.3(HGSNAT):c.235-19G>AMucopolysaccharidosis, MPS-III-C [RCV003791507]likely benign84315855643158556Human1name
405075084CV3100236single nucleotide variantNM_152419.3(HGSNAT):c.744-18T>AMucopolysaccharidosis, MPS-III-C [RCV003799789]likely benign84317229243172292Human1name
405079541CV3100514single nucleotide variantNM_152419.3(HGSNAT):c.633+17A>GMucopolysaccharidosis, MPS-III-C [RCV003800067]likely benign84316925943169259Human1name
405017232CV3100730single nucleotide variantNM_152419.3(HGSNAT):c.371+11G>CMucopolysaccharidosis, MPS-III-C [RCV003805478]likely benign84315872243158722Human1name
405176154CV3101133single nucleotide variantNM_152419.3(HGSNAT):c.1543-5T>GMucopolysaccharidosis, MPS-III-C [RCV003803520]likely benign84319766743197667Human1name
405151859CV3101911single nucleotide variantNM_152419.3(HGSNAT):c.234+20C>GMucopolysaccharidosis, MPS-III-C [RCV003801515]likely benign84314708343147083Human1name
405002392CV3102071single nucleotide variantNM_152419.3(HGSNAT):c.371+16G>CMucopolysaccharidosis, MPS-III-C [RCV003804116]likely benign84315872743158727Human1name
405005014CV3102302single nucleotide variantNM_152419.3(HGSNAT):c.743+13C>GMucopolysaccharidosis, MPS-III-C [RCV003804348]likely benign84317070743170707Human1name
405057532CV3102410single nucleotide variantNM_152419.3(HGSNAT):c.563+18G>CMucopolysaccharidosis, MPS-III-C [RCV003798552]likely benign84316152543161525Human1name
405058217CV3102465single nucleotide variantNM_152419.3(HGSNAT):c.1614-7C>TMucopolysaccharidosis, MPS-III-C [RCV003798607]likely benign84319783343197833Human1name
405060514CV3102791single nucleotide variantNM_152419.3(HGSNAT):c.371+17T>CMucopolysaccharidosis, MPS-III-C [RCV003798781]likely benign84315872843158728Human1name
405062286CV3102929single nucleotide variantNM_152419.3(HGSNAT):c.235-19G>CMucopolysaccharidosis, MPS-III-C [RCV003798920]likely benign84315855643158556Human1name
405062569CV3102951single nucleotide variantNM_152419.3(HGSNAT):c.1128+9C>AMucopolysaccharidosis, MPS-III-C [RCV003798942]likely benign84318226943182269Human1name
405064043CV3103094single nucleotide variantNM_152419.3(HGSNAT):c.633+13A>GMucopolysaccharidosis, MPS-III-C [RCV003799085]likely benign84316925543169255Human1name
405042364CV3103692single nucleotide variantNM_152419.3(HGSNAT):c.118+12C>TMucopolysaccharidosis, MPS-III-C [RCV003797410]likely benign84314062643140626Human1name
405090189CV3105064single nucleotide variantNM_152419.3(HGSNAT):c.118+13C>AMucopolysaccharidosis, MPS-III-C [RCV003800947]likely benign84314062743140627Human1name
405034738CV3105820single nucleotide variantNM_152419.3(HGSNAT):c.118+19C>TMucopolysaccharidosis, MPS-III-C [RCV003796669]likely benign84314063343140633Human1name
405041308CV3106791single nucleotide variantNM_152419.3(HGSNAT):c.851+11G>CMucopolysaccharidosis, MPS-III-C [RCV003797321]likely benign84317375443173754Human1name
405085442CV3107588single nucleotide variantNM_152419.3(HGSNAT):c.1129-9C>TMucopolysaccharidosis, MPS-III-C [RCV003800458]likely benign84319146543191465Human1name
405063123CV3108774single nucleotide variantNM_152419.3(HGSNAT):c.372-13C>TMucopolysaccharidosis, MPS-III-C [RCV003809184]likely benign84315891043158910Human1name
405010347CV3109149single nucleotide variantNM_152419.3(HGSNAT):c.118+18A>CMucopolysaccharidosis, MPS-III-C [RCV003804817]likely benign84314063243140632Human1name
405011064CV3109239single nucleotide variantNM_152419.3(HGSNAT):c.235-16G>TMucopolysaccharidosis, MPS-III-C [RCV003804907]likely benign84315855943158559Human1name
405161137CV3109849duplicationNM_152419.3(HGSNAT):c.1727-4dupMucopolysaccharidosis, MPS-III-C [RCV003802208]likely benign84319938243199383Human1name
405154781CV3110322single nucleotide variantNM_152419.3(HGSNAT):c.1614-6T>AMucopolysaccharidosis, MPS-III-C [RCV003817843]likely benign84319783443197834Human1name
405156491CV3110488single nucleotide variantNM_152419.3(HGSNAT):c.1727-5T>AMucopolysaccharidosis, MPS-III-C [RCV003818009]likely benign84319938343199383Human1name
405065903CV3110886single nucleotide variantNM_152419.3(HGSNAT):c.852-16A>GMucopolysaccharidosis, MPS-III-C [RCV003809390]likely benign84317805843178058Human1name
405154885CV3111261single nucleotide variantNM_152419.3(HGSNAT):c.1251-8C>AMucopolysaccharidosis, MPS-III-C [RCV003801717]likely benign84319229643192296Human1name
405125923CV3111890single nucleotide variantNM_152419.3(HGSNAT):c.372-12T>CMucopolysaccharidosis, MPS-III-C [RCV003815363]likely benign84315891143158911Human1name
405082717CV3113536single nucleotide variantNM_152419.3(HGSNAT):c.821-20G>TMucopolysaccharidosis, MPS-III-C [RCV003810553]likely benign84317369343173693Human1name
405037754CV3114017duplicationNM_152419.3(HGSNAT):c.1129-7dupMucopolysaccharidosis, MPS-III-C [RCV003807231]benign84319146243191463Human1name
11599510CV314513single nucleotide variantNM_152419.3(HGSNAT):c.371+15T>AMucopolysaccharidosis, MPS-III-C [RCV000266373]|Mucopolysaccharidosis, MPS-III-C [RCV003766091]likely benign|uncertain significance84315872643158726Human1name
11610632CV314597single nucleotide variantNM_152419.3(HGSNAT):c.1250+7G>AMucopolysaccharidosis, MPS-III-C [RCV000384314]|Mucopolysaccharidosis, MPS-III-C [RCV000887890]|not provided [RCV004707202]benign|likely benign|uncertain significance84319160243191602Human1name
597840139CV3867836single nucleotide variantNM_152419.3(HGSNAT):c.119-15C>TMucopolysaccharidosis, MPS-III-C [RCV005211032]likely benign84314693343146933Human1name
597910215CV3870899single nucleotide variantNM_152419.3(HGSNAT):c.494-19T>AMucopolysaccharidosis, MPS-III-C [RCV005221761]likely benign84316141943161419Human1name
597927467CV3874131single nucleotide variantNM_152419.3(HGSNAT):c.234+16C>TMucopolysaccharidosis, MPS-III-C [RCV005224403]likely benign84314707943147079Human1name
597924673CV3877347single nucleotide variantNM_152419.3(HGSNAT):c.118+11A>TMucopolysaccharidosis, MPS-III-C [RCV005224043]likely benign84314062543140625Human1name
597859487CV3878048single nucleotide variantNM_152419.3(HGSNAT):c.1543-9C>AMucopolysaccharidosis, MPS-III-C [RCV005229358]likely benign84319766343197663Human1name
597859493CV3878049single nucleotide variantNM_152419.3(HGSNAT):c.1543-8C>TMucopolysaccharidosis, MPS-III-C [RCV005229359]likely benign84319766443197664Human1name
13435139CV431722duplicationNM_152419.3(HGSNAT):c.1542+4dupMucopolysaccharidosis, MPS-III-C [RCV001339990]|Mucopolysaccharidosis, MPS-III-C [RCV001810455]|Retinal dystrophy [RCV000505003]pathogenic|likely pathogenic|uncertain significance84319702743197028Human3name
13516816CV488261single nucleotide variantNM_152419.3(HGSNAT):c.1727-9C>GMucopolysaccharidosis, MPS-III-C [RCV001083554]|Mucopolysaccharidosis, MPS-III-C [RCV001162304]|not provided [RCV000675866]|not specified [RCV000595996]benign84319937943199379Human1name
13789817CV544430single nucleotide variantNM_152419.3(HGSNAT):c.1542+1G>AMucopolysaccharidosis, MPS-III-C [RCV000674699]likely pathogenic84319702643197026Human1name
13791826CV544443single nucleotide variantNM_152419.3(HGSNAT):c.1542+1G>CMucopolysaccharidosis, MPS-III-C [RCV000667942]likely pathogenic84319702643197026Human1name
13786457CV544447single nucleotide variantNM_152419.3(HGSNAT):c.1614-2A>TMucopolysaccharidosis, MPS-III-C [RCV000672832]|Mucopolysaccharidosis, MPS-III-C [RCV001855586]|Retinal dystrophy [RCV004817902]|not provided [RCV003489791]likely pathogenic|uncertain significance84319783843197838Human3name
13785485CV544789single nucleotide variantNM_152419.3(HGSNAT):c.1542+2T>GMucopolysaccharidosis, MPS-III-C [RCV000672073]likely pathogenic84319702743197027Human1name
13790652CV544830duplicationNM_152419.3(HGSNAT):c.1012+2dupMucopolysaccharidosis, MPS-III-C [RCV000673629]uncertain significance84317823543178236Human1name
13783369CV544833single nucleotide variantNM_152419.3(HGSNAT):c.1129-2A>TMucopolysaccharidosis, MPS-III-C [RCV000670012]|Mucopolysaccharidosis, MPS-III-C [RCV001069675]likely pathogenic84319147243191472Human1name
15189583CV730577single nucleotide variantNM_152419.3(HGSNAT):c.1251-4C>TInborn genetic diseases [RCV002539370]|Mucopolysaccharidosis, MPS-III-C [RCV000887861]likely benign84319230043192300Human2name
15172467CV744365single nucleotide variantNM_152419.3(HGSNAT):c.1128+8A>GMucopolysaccharidosis, MPS-III-C [RCV000905673]likely benign84318226843182268Human1name
15161947CV759728single nucleotide variantNM_152419.3(HGSNAT):c.851+10C>TMucopolysaccharidosis, MPS-III-C [RCV001159326]|Mucopolysaccharidosis, MPS-III-C [RCV001400192]likely benign|uncertain significance84317375343173753Human1name
15164230CV779400single nucleotide variantNM_152419.3(HGSNAT):c.1129-5C>TMucopolysaccharidosis, MPS-III-C [RCV001399266]likely benign84319146943191469Human1name
28909528CV900503single nucleotide variantNM_152419.3(HGSNAT):c.1128+3G>AMucopolysaccharidosis, MPS-III-C [RCV001160689]|Mucopolysaccharidosis, MPS-III-C [RCV002557372]uncertain significance84318226343182263Human1name
38463645CV940105single nucleotide variantNM_152419.3(HGSNAT):c.1013-1G>CMucopolysaccharidosis, MPS-III-C [RCV001201450]|Retinal dystrophy [RCV003890342]pathogenic|likely pathogenic84318214443182144Human3name
38457579CV962893single nucleotide variantNM_152419.3(HGSNAT):c.1543-2A>CRetinitis pigmentosa 73 [RCV001250775]pathogenic84319767043197670Human1name
126728694CV985616single nucleotide variantNM_152419.3(HGSNAT):c.1378-1G>ASanfilippo syndrome [RCV001293488]pathogenic84319375643193756Human1name
8643412CV102395single nucleotide variantNM_152419.3(HGSNAT):c.1377+20G>AMucopolysaccharidosis, MPS-III-C [RCV000625331]|Mucopolysaccharidosis, MPS-III-C [RCV001511649]|Retinitis pigmentosa 73 [RCV001532800]|not provided [RCV000589562]|not specified [RCV000082653]benign84319245043192450Human2name
127235250CV1097085single nucleotide variantNM_152419.3(HGSNAT):c.1465-14G>AMucopolysaccharidosis, MPS-III-C [RCV001433061]likely benign84319693443196934Human1name
127313087CV1118633single nucleotide variantNM_152419.3(HGSNAT):c.1377+14G>AMucopolysaccharidosis, MPS-III-C [RCV001464606]likely benign84319244443192444Human1name
127315105CV1139516single nucleotide variantNM_152419.3(HGSNAT):c.1727-17A>GMucopolysaccharidosis, MPS-III-C [RCV001482445]likely benign84319937143199371Human1name
150410045CV1190782single nucleotide variantNM_152419.3(HGSNAT):c.1543-74A>Gnot provided [RCV001565867]likely benign84319759843197598Humanname
150470749CV1209387single nucleotide variantNM_152419.3(HGSNAT):c.821-235T>Anot provided [RCV001588498]likely benign84317347843173478Humanname
150435021CV1216037single nucleotide variantNM_152419.3(HGSNAT):c.821-276G>Anot provided [RCV001609227]benign84317343743173437Humanname
150451832CV1220914single nucleotide variantNM_152419.3(HGSNAT):c.820+123C>Tnot provided [RCV001612008]benign84317250943172509Humanname
150433041CV1231650single nucleotide variantNM_152419.3(HGSNAT):c.118+333C>Tnot provided [RCV001643312]benign84314094743140947Humanname
150454482CV1232280single nucleotide variantNM_152419.3(HGSNAT):c.234+331C>Tnot provided [RCV001648293]benign84314739443147394Humanname
150459296CV1248648single nucleotide variantNM_152419.3(HGSNAT):c.1251-47C>Tnot provided [RCV001669258]benign84319225743192257Humanname
150502377CV1254510single nucleotide variantNM_152419.3(HGSNAT):c.493+120G>Anot provided [RCV001677212]benign84315916443159164Humanname
150467471CV1255912deletionNM_152419.3(HGSNAT):c.119-164delnot provided [RCV001670546]benign84314678443146784Humanname
150474260CV1272306single nucleotide variantNM_152419.3(HGSNAT):c.633+210G>Anot provided [RCV001695844]benign84316945243169452Humanname
151836252CV1351173single nucleotide variantNM_152419.3(HGSNAT):c.1465-17T>AMucopolysaccharidosis, MPS-III-C [RCV002014818]uncertain significance84319693143196931Human1name
152055943CV1522956single nucleotide variantNM_152419.3(HGSNAT):c.1250+11C>AMucopolysaccharidosis, MPS-III-C [RCV002167433]likely benign84319160643191606Human1name
152142628CV1533214single nucleotide variantNM_152419.3(HGSNAT):c.1013-12T>GMucopolysaccharidosis, MPS-III-C [RCV002156969]likely benign84318213343182133Human1name
152064291CV1535772single nucleotide variantNM_152419.3(HGSNAT):c.1464+11A>GMucopolysaccharidosis, MPS-III-C [RCV002168412]likely benign84319385443193854Human1name
152073248CV1551800single nucleotide variantNM_152419.3(HGSNAT):c.1543-12T>GMucopolysaccharidosis, MPS-III-C [RCV002075386]likely benign84319766043197660Human1name
152116188CV1553372duplicationNM_152419.3(HGSNAT):c.1726+22dupMucopolysaccharidosis, MPS-III-C [RCV002080924]likely benign84319797143197972Human1name
152073084CV1556540single nucleotide variantNM_152419.3(HGSNAT):c.1543-11C>AMucopolysaccharidosis, MPS-III-C [RCV002111725]likely benign84319766143197661Human1name
152107481CV1560269single nucleotide variantNM_152419.3(HGSNAT):c.1013-20C>TMucopolysaccharidosis, MPS-III-C [RCV002134043]likely benign84318212543182125Human1name
152069063CV1562222single nucleotide variantNM_152419.3(HGSNAT):c.1727-11C>GMucopolysaccharidosis, MPS-III-C [RCV002169054]likely benign84319937743199377Human1name
152139364CV1562806single nucleotide variantNM_152419.3(HGSNAT):c.1542+18C>TMucopolysaccharidosis, MPS-III-C [RCV002100555]likely benign84319704343197043Human1name
152124538CV1563278single nucleotide variantNM_152419.3(HGSNAT):c.1542+20C>TMucopolysaccharidosis, MPS-III-C [RCV002118275]benign84319704543197045Human1name
152051405CV1569266single nucleotide variantNM_152419.3(HGSNAT):c.1726+17C>TMucopolysaccharidosis, MPS-III-C [RCV002207566]likely benign84319796943197969Human1name
152167424CV1577441single nucleotide variantNM_152419.3(HGSNAT):c.1465-16G>AMucopolysaccharidosis, MPS-III-C [RCV002204702]likely benign84319693243196932Human1name
152170718CV1592551single nucleotide variantNM_152419.3(HGSNAT):c.1727-19G>CMucopolysaccharidosis, MPS-III-C [RCV002161864]likely benign84319936943199369Human1name
152067668CV1600273single nucleotide variantNM_152419.3(HGSNAT):c.1727-15G>AMucopolysaccharidosis, MPS-III-C [RCV002111010]likely benign84319937343199373Human1name
152106343CV1609046single nucleotide variantNM_152419.3(HGSNAT):c.1727-13C>GMucopolysaccharidosis, MPS-III-C [RCV002096217]likely benign84319937543199375Human1name
152140736CV1609132single nucleotide variantNM_152419.3(HGSNAT):c.1250+10C>TMucopolysaccharidosis, MPS-III-C [RCV002200541]likely benign84319160543191605Human1name
152175427CV1614252single nucleotide variantNM_152419.3(HGSNAT):c.1727-17A>TMucopolysaccharidosis, MPS-III-C [RCV002163561]likely benign84319937143199371Human1name
152036253CV1617492single nucleotide variantNM_152419.3(HGSNAT):c.1250+12C>TMucopolysaccharidosis, MPS-III-C [RCV002125375]likely benign84319160743191607Human1name
152042179CV1619575single nucleotide variantNM_152419.3(HGSNAT):c.1251-16C>GMucopolysaccharidosis, MPS-III-C [RCV002188410]likely benign84319228843192288Human1name
152086278CV1633721single nucleotide variantNM_152419.3(HGSNAT):c.1727-19G>AMucopolysaccharidosis, MPS-III-C [RCV002113432]likely benign84319936943199369Human1name
152073109CV1637944single nucleotide variantNM_152419.3(HGSNAT):c.1378-20T>GMucopolysaccharidosis, MPS-III-C [RCV002192055]likely benign84319373743193737Human1name
152062318CV1638573single nucleotide variantNM_152419.3(HGSNAT):c.1543-16C>TMucopolysaccharidosis, MPS-III-C [RCV002073823]likely benign84319765643197656Human1name
152099571CV1655078single nucleotide variantNM_152419.3(HGSNAT):c.1543-20C>AMucopolysaccharidosis, MPS-III-C [RCV002115147]likely benign84319765243197652Human1name
152033447CV1658077single nucleotide variantNM_152419.3(HGSNAT):c.1614-13C>TMucopolysaccharidosis, MPS-III-C [RCV002187090]likely benign84319782743197827Human1name
152145385CV1658330single nucleotide variantNM_152419.3(HGSNAT):c.1377+19C>TMucopolysaccharidosis, MPS-III-C [RCV002219961]likely benign84319244943192449Human1name
152166709CV1661374single nucleotide variantNM_152419.3(HGSNAT):c.1378-13T>GMucopolysaccharidosis, MPS-III-C [RCV002124276]likely benign84319374443193744Human1name
155265026CV1704566single nucleotide variantNM_152419.3(HGSNAT):c.118+221G>Tnot provided [RCV002284782]likely benign84314083543140835Humanname
155267836CV1705179single nucleotide variantNM_152419.3(HGSNAT):c.493+836G>Anot provided [RCV002285784]likely benign84315988043159880Humanname
156269931CV1870654single nucleotide variantNM_152419.3(HGSNAT):c.1543-10C>GMucopolysaccharidosis, MPS-III-C [RCV003060677]likely benign84319766243197662Human1name
156153888CV1875297single nucleotide variantNM_152419.3(HGSNAT):c.1377+13C>TMucopolysaccharidosis, MPS-III-C [RCV003056634]likely benign84319244343192443Human1name
156222246CV1879364single nucleotide variantNM_152419.3(HGSNAT):c.1129-10C>AMucopolysaccharidosis, MPS-III-C [RCV003058987]likely benign84319146443191464Human1name
156351987CV1883257single nucleotide variantNM_152419.3(HGSNAT):c.1542+12G>AMucopolysaccharidosis, MPS-III-C [RCV003091050]likely benign84319703743197037Human1name
156413668CV1905349single nucleotide variantNM_152419.3(HGSNAT):c.1250+17G>TMucopolysaccharidosis, MPS-III-C [RCV003073390]likely benign84319161243191612Human1name
156365552CV1908417single nucleotide variantNM_152419.3(HGSNAT):c.1614-20G>AMucopolysaccharidosis, MPS-III-C [RCV002582037]likely benign84319782043197820Human1name
156414020CV1915602single nucleotide variantNM_152419.3(HGSNAT):c.1377+13C>AMucopolysaccharidosis, MPS-III-C [RCV002588358]likely benign84319244343192443Human1name
156130569CV2037410single nucleotide variantNM_152419.3(HGSNAT):c.1614-11A>GMucopolysaccharidosis, MPS-III-C [RCV002800597]likely benign84319782943197829Human1name
155936397CV2114198single nucleotide variantNM_152419.3(HGSNAT):c.1464+17T>CMucopolysaccharidosis, MPS-III-C [RCV002904167]likely benign84319386043193860Human1name
156377383CV2189162single nucleotide variantNM_152419.3(HGSNAT):c.1726+10C>TMucopolysaccharidosis, MPS-III-C [RCV003050221]likely benign84319796243197962Human1name
156144669CV2190214single nucleotide variantNM_152419.3(HGSNAT):c.1464+10C>AMucopolysaccharidosis, MPS-III-C [RCV003056315]likely benign84319385343193853Human1name
405006105CV3082806single nucleotide variantNM_152419.3(HGSNAT):c.1727-11C>TMucopolysaccharidosis, MPS-III-C [RCV003783906]likely benign84319937743199377Human1name
405007604CV3083116single nucleotide variantNM_152419.3(HGSNAT):c.1726+13C>TMucopolysaccharidosis, MPS-III-C [RCV003784063]likely benign84319796543197965Human1name
405010823CV3083377single nucleotide variantNM_152419.3(HGSNAT):c.1250+16G>AMucopolysaccharidosis, MPS-III-C [RCV003784324]likely benign84319161143191611Human1name
405025930CV3085070single nucleotide variantNM_152419.3(HGSNAT):c.1726+14A>GMucopolysaccharidosis, MPS-III-C [RCV003795936]likely benign84319796643197966Human1name
404999300CV3085897single nucleotide variantNM_152419.3(HGSNAT):c.1543-19C>TMucopolysaccharidosis, MPS-III-C [RCV003783267]likely benign84319765343197653Human1name
402518070CV3086084single nucleotide variantNM_152419.3(HGSNAT):c.1012+14C>TMucopolysaccharidosis, MPS-III-C [RCV003780855]likely benign84317824843178248Human1name
404984628CV3087284single nucleotide variantNM_152419.3(HGSNAT):c.1464+11A>CMucopolysaccharidosis, MPS-III-C [RCV003781747]likely benign84319385443193854Human1name
404996621CV3088531deletionNM_152419.3(HGSNAT):c.1465-19delMucopolysaccharidosis, MPS-III-C [RCV003793308]likely benign84319692943196929Human1name
404993464CV3089056deletionNM_152419.3(HGSNAT):c.1251-12delMucopolysaccharidosis, MPS-III-C [RCV003782702]benign84319228943192289Human1name
404993561CV3089067single nucleotide variantNM_152419.3(HGSNAT):c.1250+14T>CMucopolysaccharidosis, MPS-III-C [RCV003782713]likely benign84319160943191609Human1name
402510245CV3089202single nucleotide variantNM_152419.3(HGSNAT):c.1465-18C>TMucopolysaccharidosis, MPS-III-C [RCV003780234]likely benign84319693043196930Human1name
402516983CV3089893duplicationNM_152419.3(HGSNAT):c.1250+19dupMucopolysaccharidosis, MPS-III-C [RCV003780771]benign84319160943191610Human1name
402503940CV3090129single nucleotide variantNM_152419.3(HGSNAT):c.1128+13G>AMucopolysaccharidosis, MPS-III-C [RCV003788896]likely benign84318227343182273Human1name
402489833CV3090920single nucleotide variantNM_152419.3(HGSNAT):c.1377+14G>CMucopolysaccharidosis, MPS-III-C [RCV003787422]likely benign84319244443192444Human1name
402491790CV3091110single nucleotide variantNM_152419.3(HGSNAT):c.1012+14C>AMucopolysaccharidosis, MPS-III-C [RCV003787615]likely benign84317824843178248Human1name
405018065CV3091662single nucleotide variantNM_152419.3(HGSNAT):c.1012+15C>TMucopolysaccharidosis, MPS-III-C [RCV003795329]likely benign84317824943178249Human1name
402517692CV3091752single nucleotide variantNM_152419.3(HGSNAT):c.1012+19T>CMucopolysaccharidosis, MPS-III-C [RCV003790198]likely benign84317825343178253Human1name
402521695CV3092034single nucleotide variantNM_152419.3(HGSNAT):c.1377+15A>TMucopolysaccharidosis, MPS-III-C [RCV003790480]likely benign84319244543192445Human1name
405028164CV3094856single nucleotide variantNM_152419.3(HGSNAT):c.1726+15A>GMucopolysaccharidosis, MPS-III-C [RCV003796218]likely benign84319796743197967Human1name
405056467CV3095158single nucleotide variantNM_152419.3(HGSNAT):c.1614-16C>TMucopolysaccharidosis, MPS-III-C [RCV003798472]likely benign84319782443197824Human1name
405002406CV3095585single nucleotide variantNM_152419.3(HGSNAT):c.1251-14T>CMucopolysaccharidosis, MPS-III-C [RCV003793889]likely benign84319229043192290Human1name
405003315CV3095669single nucleotide variantNM_152419.3(HGSNAT):c.1543-10C>TMucopolysaccharidosis, MPS-III-C [RCV003793974]likely benign84319766243197662Human1name
405009925CV3096582single nucleotide variantNM_152419.3(HGSNAT):c.1378-17T>CMucopolysaccharidosis, MPS-III-C [RCV003794571]likely benign84319374043193740Human1name
405010221CV3096611single nucleotide variantNM_152419.3(HGSNAT):c.1727-20T>CMucopolysaccharidosis, MPS-III-C [RCV003794600]likely benign84319936843199368Human1name
405024815CV3097713single nucleotide variantNM_152419.3(HGSNAT):c.1128+11A>GMucopolysaccharidosis, MPS-III-C [RCV003806174]likely benign84318227143182271Human1name
405071105CV3099845single nucleotide variantNM_152419.3(HGSNAT):c.1250+15G>CMucopolysaccharidosis, MPS-III-C [RCV003799560]likely benign84319161043191610Human1name
405021259CV3101284single nucleotide variantNM_152419.3(HGSNAT):c.1465-15T>CMucopolysaccharidosis, MPS-III-C [RCV003805863]likely benign84319693343196933Human1name
404977363CV3102672single nucleotide variantNM_152419.3(HGSNAT):c.1013-12T>CMucopolysaccharidosis, MPS-III-C [RCV003790766]likely benign84318213343182133Human1name
405151462CV3105744single nucleotide variantNM_152419.3(HGSNAT):c.1250+18G>AMucopolysaccharidosis, MPS-III-C [RCV003801461]likely benign84319161343191613Human1name
405014349CV3106622single nucleotide variantNM_152419.3(HGSNAT):c.1377+15A>GMucopolysaccharidosis, MPS-III-C [RCV003794959]likely benign84319244543192445Human1name
405058152CV3108221single nucleotide variantNM_152419.3(HGSNAT):c.1128+14T>AMucopolysaccharidosis, MPS-III-C [RCV003808799]likely benign84318227443182274Human1name
405009992CV3109117single nucleotide variantNM_152419.3(HGSNAT):c.1128+16T>CMucopolysaccharidosis, MPS-III-C [RCV003804785]likely benign84318227643182276Human1name
405157056CV3109391single nucleotide variantNM_152419.3(HGSNAT):c.1614-18C>GMucopolysaccharidosis, MPS-III-C [RCV003801915]likely benign84319782243197822Human1name
405160451CV3109792single nucleotide variantNM_152419.3(HGSNAT):c.1726+18T>GMucopolysaccharidosis, MPS-III-C [RCV003802151]likely benign84319797043197970Human1name
405154795CV3110323single nucleotide variantNM_152419.3(HGSNAT):c.1377+11C>GMucopolysaccharidosis, MPS-III-C [RCV003817844]likely benign84319244143192441Human1name
405126894CV3111995single nucleotide variantNM_152419.3(HGSNAT):c.1726+15A>CMucopolysaccharidosis, MPS-III-C [RCV003815468]likely benign84319796743197967Human1name
405108636CV3112353single nucleotide variantNM_152419.3(HGSNAT):c.1250+10C>AMucopolysaccharidosis, MPS-III-C [RCV003813196]likely benign84319160543191605Human1name
597840988CV3864596single nucleotide variantNM_152419.3(HGSNAT):c.1614-12C>TMucopolysaccharidosis, MPS-III-C [RCV005211207]likely benign84319782843197828Human1name
597897543CV3866184single nucleotide variantNM_152419.3(HGSNAT):c.1464+16A>TMucopolysaccharidosis, MPS-III-C [RCV005219801]likely benign84319385943193859Human1name
597910100CV3870884single nucleotide variantNM_152419.3(HGSNAT):c.1251-16C>TMucopolysaccharidosis, MPS-III-C [RCV005221746]likely benign84319228843192288Human1name
597888445CV3871140single nucleotide variantNM_152419.3(HGSNAT):c.1129-11C>TMucopolysaccharidosis, MPS-III-C [RCV005218472]likely benign84319146343191463Human1name
597899291CV3876185single nucleotide variantNM_152419.3(HGSNAT):c.1614-17T>CMucopolysaccharidosis, MPS-III-C [RCV005220075]likely benign84319782343197823Human1name
14746354CV663400single nucleotide variantNM_152419.3(HGSNAT):c.633+240T>Gnot provided [RCV000844355]benign84316948243169482Humanname
15112940CV775276single nucleotide variantNM_152419.3(HGSNAT):c.1012+10T>AMucopolysaccharidosis, MPS-III-C [RCV000939035]likely benign84317824443178244Human1name
15103670CV775334single nucleotide variantNM_152419.3(HGSNAT):c.1614-10C>TMucopolysaccharidosis, MPS-III-C [RCV001275635]|Mucopolysaccharidosis, MPS-III-C [RCV002068693]likely benign|uncertain significance84319783043197830Human1name
38477139CV940106single nucleotide variantNM_152419.3(HGSNAT):c.1465-10T>CMucopolysaccharidosis, MPS-III-C [RCV001204954]|Mucopolysaccharidosis, MPS-III-C [RCV001828645]uncertain significance84319693843196938Human1name
38597977CV963083single nucleotide variantNM_152419.3(HGSNAT):c.493+809T>CMucopolysaccharidosis, MPS-III-C [RCV001251050]pathogenic84315985343159853Human1name
150405962CV1190783single nucleotide variantNM_152419.3(HGSNAT):c.1727-106T>Gnot provided [RCV001564527]likely benign84319928243199282Humanname
150464952CV1200996duplicationNM_152419.3(HGSNAT):c.1250+342dupnot provided [RCV001587476]likely benign84319192743191928Humanname
150459976CV1203003single nucleotide variantNM_152419.3(HGSNAT):c.1464+145G>Anot provided [RCV001586656]likely benign84319398843193988Humanname
150433995CV1243841single nucleotide variantNM_152419.3(HGSNAT):c.1251-130C>Tnot provided [RCV001665047]benign84319217443192174Humanname
150444317CV1249399duplicationNM_152419.3(HGSNAT):c.1464+216dupnot provided [RCV001666831]benign84319405243194053Humanname
150487882CV1251589single nucleotide variantNM_152419.3(HGSNAT):c.1251-289G>Anot provided [RCV001674260]benign84319201543192015Humanname
150498857CV1270723single nucleotide variantNM_152419.3(HGSNAT):c.1251-220A>Gnot provided [RCV001689272]benign84319208443192084Humanname
405275484CV3215945single nucleotide variantNM_152419.3(HGSNAT):c.1465-473T>CHGSNAT-related disorder [RCV003952230]likely benign84319647543196475Humanname , trait , alternate_id
14746367CV663358single nucleotide variantNM_152419.3(HGSNAT):c.1251-291G>Cnot provided [RCV000844370]benign84319201343192013Humanname
14746365CV663401single nucleotide variantNM_152419.3(HGSNAT):c.1129-222G>Anot provided [RCV000844368]benign84319125243191252Humanname
152038381CV1642128microsatelliteNM_152419.3(HGSNAT):c.1727-14TC[3]Mucopolysaccharidosis, MPS-III-C [RCV002107367]likely benign84319937443199375Humanname
127334643CV1139507microsatelliteNM_152419.3(HGSNAT):c.744-5_744-3delMucopolysaccharidosis, MPS-III-C [RCV001490983]likely benign84317230043172302Humanname
402518084CV3086085microsatelliteNM_152419.3(HGSNAT):c.564-8_564-5delMucopolysaccharidosis, MPS-III-C [RCV003780856]likely benign84316915843169161Humanname
11655894CV309284deletionNM_152419.3(HGSNAT):c.*1100_*1103delSanfilippo syndrome [RCV000329375]uncertain significance84320066643200669Human1name
597865949CV3872594deletionNM_152419.3(HGSNAT):c.1129-11_1134delMucopolysaccharidosis, MPS-III-C [RCV005214869]likely pathogenic84319146243191478Human1name
34895539CV917464deletionNM_152419.3(HGSNAT):c.118+67_118+90delnot specified [RCV001192637]uncertain significance84314067143140694Humanname
150502002CV1255172deletionNM_152419.3(HGSNAT):c.564-112_564-109delnot provided [RCV001677091]benign84316905843169061Humanname
156445330CV1945411microsatelliteNM_152419.3(HGSNAT):c.1464+14_1464+18delMucopolysaccharidosis, MPS-III-C [RCV003116271]likely benign84319385143193855Humanname
405011410CV3113917deletionNM_152419.3(HGSNAT):c.1013-15_1013-14delMucopolysaccharidosis, MPS-III-C [RCV003804939]likely benign84318213043182131Human1name
155989098CV2026829indelNM_152419.3(HGSNAT):c.1465-4_1465-3delinsGAMucopolysaccharidosis, MPS-III-C [RCV002755670]uncertain significance84319694443196945Humanname
13519617CV487394duplicationNM_152419.2(HGSNAT):c.-115_-101dupTCAGGCGGCGGTGACnot specified [RCV000780344]uncertain significance84314037343140374Humanname
151755061CV1453920indelNM_152419.3(HGSNAT):c.1543-20_1543-7delinsTTTCTGAGATAATAATATAAAATGMucopolysaccharidosis, MPS-III-C [RCV001913369]uncertain significance84319765243197665Humanname
127272954CV1097074single nucleotide variantNM_152419.3(HGSNAT):c.666C>T (p.Leu222=)HGSNAT-related disorder [RCV004751982]|Mucopolysaccharidosis, MPS-III-C [RCV001442379]likely benign84317061743170617Human2name , alternate_id
127327975CV1118619single nucleotide variantNM_152419.3(HGSNAT):c.288T>C (p.Pro96=)HGSNAT-related disorder [RCV003965938]|Mucopolysaccharidosis, MPS-III-C [RCV001469370]likely benign84315862843158628Human2name , alternate_id
127299635CV1118626single nucleotide variantNM_152419.3(HGSNAT):c.840C>T (p.Leu280=)HGSNAT-related disorder [RCV003938852]|Mucopolysaccharidosis, MPS-III-C [RCV001478247]likely benign84317373243173732Human2name , alternate_id
151741143CV1404826single nucleotide variantNM_152419.3(HGSNAT):c.995A>G (p.Asn332Ser)HGSNAT-related disorder [RCV004752078]|Mucopolysaccharidosis, MPS-III-C [RCV001947112]uncertain significance84317821743178217Human2alternate_id
10401627CV205377single nucleotide variantNM_152419.3(HGSNAT):c.1843G>A (p.Ala615Thr)HGSNAT-related disorder [RCV003407694]|Mucopolysaccharidosis, MPS-III-C [RCV000190845]|Mucopolysaccharidosis, MPS-III-C [RCV001082167]|Retinal dystrophy [RCV000504631]|Retinitis pigmentosa 73 [RCV000190844]|Retinitis pigmentosa [RCV001003049]|not provided [RCV00pathogenic|likely pathogenic|benign|likely benign|conflicting interpretations of pathogenicity|uncertain significance84319950443199504Human6alternate_id
10401628CV205378single nucleotide variantNM_152419.3(HGSNAT):c.1209G>T (p.Trp403Cys)HGSNAT-related disorder [RCV003417693]|Mucopolysaccharidosis, MPS-III-C [RCV000190846]|Mucopolysaccharidosis, MPS-III-C [RCV002500583]pathogenic|conflicting interpretations of pathogenicity|uncertain significance84319155443191554Human2alternate_id
401934716CV2802777duplicationNM_152419.3(HGSNAT):c.416dup (p.Asn141fs)HGSNAT-related disorder [RCV003412142]likely pathogenic84315896643158967Humanname , trait , alternate_id
11646964CV314506single nucleotide variantNM_152419.3(HGSNAT):c.108G>A (p.Ala36=)HGSNAT-related disorder [RCV003932503]|Mucopolysaccharidosis, MPS-III-C [RCV000273849]|Mucopolysaccharidosis, MPS-III-C [RCV001083544]|not provided [RCV000675862]|not specified [RCV001699401]benign|likely benign|uncertain significance84314060443140604Human2name , alternate_id
408377575CV3509541single nucleotide variantNM_152419.3(HGSNAT):c.1375G>A (p.Ala459Thr)HGSNAT-related disorder [RCV004751091]uncertain significance84319242843192428Humantrait , alternate_id
408378803CV3516351single nucleotide variantNM_152419.3(HGSNAT):c.1029G>A (p.Val343=)HGSNAT-related disorder [RCV004752447]likely benign84318216143182161Humanname , trait , alternate_id
12898892CV407394single nucleotide variantNM_152419.3(HGSNAT):c.1880A>G (p.Tyr627Cys)HGSNAT-related disorder [RCV004751559]|Inborn genetic diseases [RCV002526563]|Intellectual disability [RCV001252520]|Mucopolysaccharidosis, MPS-III-C [RCV000625332]|Mucopolysaccharidosis, MPS-III-C [RCV000802522]|Retinal dystrophy [RCV004816691]|not provided [RClikely benign|uncertain significance84319954143199541Human7alternate_id
15148850CV711545single nucleotide variantNM_152419.3(HGSNAT):c.689C>T (p.Thr230Met)HGSNAT-related disorder [RCV003905933]|Mucopolysaccharidosis, MPS-III-C [RCV000967634]|Mucopolysaccharidosis, MPS-III-C [RCV001159323]|Retinal dystrophy [RCV003890124]benign|likely benign84317064043170640Human4alternate_id
15157528CV723110single nucleotide variantNM_152419.3(HGSNAT):c.828A>G (p.Thr276=)HGSNAT-related disorder [RCV003948307]|Mucopolysaccharidosis, MPS-III-C [RCV000880835]|Mucopolysaccharidosis, MPS-III-C [RCV001275629]|not specified [RCV001805927]benign|likely benign84317372043173720Human2name , alternate_id
15103318CV723113single nucleotide variantNM_152419.3(HGSNAT):c.1250C>T (p.Thr417Ile)HGSNAT-related disorder [RCV003950410]|Inborn genetic diseases [RCV004028422]|Mucopolysaccharidosis, MPS-III-C [RCV000892647]|Mucopolysaccharidosis, MPS-III-C [RCV001275632]|Retinal dystrophy [RCV003890021]|not provided [RCV004792572]|not specified [RCV003994149benign|likely benign|uncertain significance84319159543191595Human5alternate_id
15107181CV723114single nucleotide variantNM_152419.3(HGSNAT):c.1752C>T (p.Val584=)HGSNAT-related disorder [RCV003957995]|Mucopolysaccharidosis, MPS-III-C [RCV000893424]|Mucopolysaccharidosis, MPS-III-C [RCV001825800]likely benign84319941343199413Human2name , alternate_id
15103323CV723115single nucleotide variantNM_152419.3(HGSNAT):c.1759G>A (p.Glu587Lys)HGSNAT-related disorder [RCV003940720]|Inborn genetic diseases [RCV002540108]|Mucopolysaccharidosis, MPS-III-C [RCV000892648]|Mucopolysaccharidosis, MPS-III-C [RCV001275637]|not provided [RCV004792573]|not specified [RCV003994150]likely benign|uncertain significance84319942043199420Human3alternate_id
15170174CV751178single nucleotide variantNM_152419.3(HGSNAT):c.1635G>A (p.Thr545=)HGSNAT-related disorder [RCV003903069]|Mucopolysaccharidosis, MPS-III-C [RCV000927644]likely benign84319786143197861Human2name , alternate_id
26916988CV834786single nucleotide variantNM_152419.3(HGSNAT):c.887C>T (p.Ser296Leu)HGSNAT-related disorder [RCV003963005]|Mucopolysaccharidosis, MPS-III-C [RCV001042356]|Mucopolysaccharidosis, MPS-III-C [RCV001275630]|Retinal dystrophy [RCV004813581]|Retinitis pigmentosa 73 [RCV001250771]|not specified [RCV004768802]likely pathogenic|uncertain significance84317810943178109Human4name , alternate_id
38478522CV934321single nucleotide variantNM_152419.3(HGSNAT):c.691T>C (p.Trp231Arg)HGSNAT-related disorder [RCV004751914]|Inborn genetic diseases [RCV004033651]|Mucopolysaccharidosis, MPS-III-C [RCV001205587]|Mucopolysaccharidosis, MPS-III-C [RCV001836137]uncertain significance84317064243170642Human3name , alternate_id
38499012CV955422single nucleotide variantNM_152419.3(HGSNAT):c.32T>C (p.Leu11Pro)HGSNAT-related disorder [RCV004751938]|Inborn genetic diseases [RCV002568577]|Mucopolysaccharidosis, MPS-III-C [RCV001244177]|Mucopolysaccharidosis, MPS-III-C [RCV001829921]|not provided [RCV003481024]uncertain significance84314052843140528Human3name , alternate_id
152085632CV1617350single nucleotide variantNM_152419.3(HGSNAT):c.6C>T (p.Ser2=)Mucopolysaccharidosis, MPS-III-C [RCV002076945]likely benign84314050243140502Human1name
404978611CV3099069single nucleotide variantNM_152419.3(HGSNAT):c.9G>A (p.Gly3=)Mucopolysaccharidosis, MPS-III-C [RCV003791049]likely benign84314050543140505Human1name
127310475CV1139493single nucleotide variantNM_152419.3(HGSNAT):c.12G>T (p.Ala4=)Mucopolysaccharidosis, MPS-III-C [RCV001481147]likely benign84314050843140508Human1name
152109006CV1563803single nucleotide variantNM_152419.3(HGSNAT):c.21G>A (p.Ala7=)Mucopolysaccharidosis, MPS-III-C [RCV002174088]likely benign84314051743140517Human1name
152121081CV1574387single nucleotide variantNM_152419.3(HGSNAT):c.27C>A (p.Ala9=)Mucopolysaccharidosis, MPS-III-C [RCV002175586]likely benign84314052343140523Human1name
152150595CV1661554single nucleotide variantNM_152419.3(HGSNAT):c.12G>C (p.Ala4=)Mucopolysaccharidosis, MPS-III-C [RCV002179387]likely benign84314050843140508Human1name
402504592CV3088750single nucleotide variantNM_152419.3(HGSNAT):c.18G>A (p.Arg6=)Mucopolysaccharidosis, MPS-III-C [RCV003779459]likely benign84314051443140514Human1name
597879447CV3872046single nucleotide variantNM_152419.3(HGSNAT):c.22C>T (p.Leu8=)Mucopolysaccharidosis, MPS-III-C [RCV005217098]likely benign84314051843140518Human1name
15117852CV766827single nucleotide variantNM_152419.3(HGSNAT):c.12G>A (p.Ala4=)Mucopolysaccharidosis, MPS-III-C [RCV000939905]|Mucopolysaccharidosis, MPS-III-C [RCV001273608]likely benign|uncertain significance84314050843140508Human1name
126770285CV1028559single nucleotide variantNM_152419.3(HGSNAT):c.7G>C (p.Gly3Arg)Mucopolysaccharidosis, MPS-III-C [RCV001344388]uncertain significance84314050343140503Human1name
127279617CV1075389single nucleotide variantNM_152419.3(HGSNAT):c.39G>C (p.Leu13=)Mucopolysaccharidosis, MPS-III-C [RCV001409245]|Mucopolysaccharidosis, MPS-III-C [RCV001831443]likely benign84314053543140535Human1name
127258691CV1075390single nucleotide variantNM_152419.3(HGSNAT):c.48C>G (p.Ser16=)Mucopolysaccharidosis, MPS-III-C [RCV001419602]likely benign84314054443140544Human1name
127283450CV1075391single nucleotide variantNM_152419.3(HGSNAT):c.66G>A (p.Leu22=)Mucopolysaccharidosis, MPS-III-C [RCV001411820]likely benign84314056243140562Human1name
127236074CV1075392single nucleotide variantNM_152419.3(HGSNAT):c.72C>T (p.Ala24=)Mucopolysaccharidosis, MPS-III-C [RCV001392011]likely benign84314056843140568Human1name
127275804CV1097061single nucleotide variantNM_152419.3(HGSNAT):c.45G>A (p.Ala15=)Mucopolysaccharidosis, MPS-III-C [RCV001432523]likely benign84314054143140541Human1name
127257393CV1097062single nucleotide variantNM_152419.3(HGSNAT):c.60C>T (p.Ala20=)Mucopolysaccharidosis, MPS-III-C [RCV001427103]|Mucopolysaccharidosis, MPS-III-C [RCV001836400]|Retinal dystrophy [RCV003888134]likely benign84314055643140556Human3name
127268619CV1097063single nucleotide variantNM_152419.3(HGSNAT):c.90G>T (p.Gly30=)Mucopolysaccharidosis, MPS-III-C [RCV001440833]likely benign84314058643140586Human1name
127319376CV1118612single nucleotide variantNM_152419.3(HGSNAT):c.90G>C (p.Gly30=)Mucopolysaccharidosis, MPS-III-C [RCV001466525]likely benign84314058643140586Human1name
127324138CV1139494single nucleotide variantNM_152419.3(HGSNAT):c.69G>A (p.Leu23=)Mucopolysaccharidosis, MPS-III-C [RCV001485410]likely benign84314056543140565Human1name
127315897CV1139495single nucleotide variantNM_152419.3(HGSNAT):c.78C>T (p.Gly26=)Mucopolysaccharidosis, MPS-III-C [RCV001502864]likely benign84314057443140574Human1name
152171719CV1575590single nucleotide variantNM_152419.3(HGSNAT):c.45G>C (p.Ala15=)Mucopolysaccharidosis, MPS-III-C [RCV002183594]likely benign84314054143140541Human1name
152127623CV1598578single nucleotide variantNM_152419.3(HGSNAT):c.67C>T (p.Leu23=)Mucopolysaccharidosis, MPS-III-C [RCV002155088]likely benign84314056343140563Human1name
152035484CV1604179single nucleotide variantNM_152419.3(HGSNAT):c.37C>T (p.Leu13=)Mucopolysaccharidosis, MPS-III-C [RCV002087136]likely benign84314053343140533Human1name
152122795CV1613603single nucleotide variantNM_152419.3(HGSNAT):c.99C>A (p.Ala33=)Mucopolysaccharidosis, MPS-III-C [RCV002081788]likely benign84314059543140595Human1name
152164231CV1619733single nucleotide variantNM_152419.3(HGSNAT):c.51G>A (p.Val17=)Mucopolysaccharidosis, MPS-III-C [RCV002181493]likely benign84314054743140547Human1name
152165867CV1661045single nucleotide variantNM_152419.3(HGSNAT):c.64C>T (p.Leu22=)Mucopolysaccharidosis, MPS-III-C [RCV002124106]likely benign84314056043140560Human1name
156352048CV1870203single nucleotide variantNM_152419.3(HGSNAT):c.99C>T (p.Ala33=)Mucopolysaccharidosis, MPS-III-C [RCV003064933]likely benign84314059543140595Human1name
156021674CV1882375single nucleotide variantNM_152419.3(HGSNAT):c.42C>T (p.Ala14=)Mucopolysaccharidosis, MPS-III-C [RCV003077651]likely benign84314053843140538Human1name
155956897CV1903568single nucleotide variantNM_152419.3(HGSNAT):c.8G>C (p.Gly3Ala)Mucopolysaccharidosis, MPS-III-C [RCV003095635]uncertain significance84314050443140504Human1name
155993639CV2023443single nucleotide variantNM_152419.3(HGSNAT):c.48C>T (p.Ser16=)Mucopolysaccharidosis, MPS-III-C [RCV002755860]likely benign84314054443140544Human1name
155994829CV2023531single nucleotide variantNM_152419.3(HGSNAT):c.42C>A (p.Ala14=)Mucopolysaccharidosis, MPS-III-C [RCV002755913]likely benign84314053843140538Human1name
156013865CV2038490single nucleotide variantNM_152419.3(HGSNAT):c.93C>T (p.Arg31=)Mucopolysaccharidosis, MPS-III-C [RCV002780290]likely benign84314058943140589Human1name
155929650CV2041745single nucleotide variantNM_152419.3(HGSNAT):c.6C>A (p.Ser2Arg)Inborn genetic diseases [RCV002751092]|Mucopolysaccharidosis, MPS-III-C [RCV002751093]benign|uncertain significance84314050243140502Human2name
155978469CV2073227deletionNM_152419.3(HGSNAT):c.10del (p.Ala4fs)Mucopolysaccharidosis, MPS-III-C [RCV002842403]pathogenic84314050343140503Human1name
156075039CV2102172single nucleotide variantNM_152419.3(HGSNAT):c.75C>T (p.Pro25=)Mucopolysaccharidosis, MPS-III-C [RCV002912509]likely benign84314057143140571Human1name
405021328CV3085635single nucleotide variantNM_152419.3(HGSNAT):c.81C>T (p.Gly27=)Mucopolysaccharidosis, MPS-III-C [RCV003785358]likely benign84314057743140577Human1name
402507792CV3090660single nucleotide variantNM_152419.3(HGSNAT):c.93C>G (p.Arg31=)Mucopolysaccharidosis, MPS-III-C [RCV003789276]likely benign84314058943140589Human1name
404979447CV3099421single nucleotide variantNM_152419.3(HGSNAT):c.34C>T (p.Leu12=)Mucopolysaccharidosis, MPS-III-C [RCV003791249]likely benign84314053043140530Human1name
405064080CV3103097single nucleotide variantNM_152419.3(HGSNAT):c.54G>A (p.Leu18=)Mucopolysaccharidosis, MPS-III-C [RCV003799088]likely benign84314055043140550Human1name
405016299CV3106931single nucleotide variantNM_152419.3(HGSNAT):c.30G>A (p.Ala10=)Mucopolysaccharidosis, MPS-III-C [RCV003795101]|Retinal dystrophy [RCV003889341]likely pathogenic|likely benign84314052643140526Human3name
405128112CV3112133single nucleotide variantNM_152419.3(HGSNAT):c.57C>T (p.Ser19=)Mucopolysaccharidosis, MPS-III-C [RCV003815607]likely benign84314055343140553Human1name
597853551CV3869782single nucleotide variantNM_152419.3(HGSNAT):c.66G>C (p.Leu22=)Mucopolysaccharidosis, MPS-III-C [RCV005213067]likely benign84314056243140562Human1name
15110706CV766828single nucleotide variantNM_152419.3(HGSNAT):c.87G>C (p.Ser29=)Mucopolysaccharidosis, MPS-III-C [RCV000938603]likely benign84314058343140583Human1name
15136345CV766829single nucleotide variantNM_152419.3(HGSNAT):c.99C>G (p.Ala33=)Mucopolysaccharidosis, MPS-III-C [RCV001485239]likely benign84314059543140595Human1name
28867959CV899646single nucleotide variantNM_152419.3(HGSNAT):c.63G>A (p.Ala21=)Mucopolysaccharidosis, MPS-III-C [RCV001162199]|Mucopolysaccharidosis, MPS-III-C [RCV001515411]benign84314055943140559Human1name
126757380CV1028561single nucleotide variantNM_152419.3(HGSNAT):c.204C>A (p.Thr68=)Mucopolysaccharidosis, MPS-III-C [RCV001339549]|Mucopolysaccharidosis, MPS-III-C [RCV001830413]likely benign|uncertain significance84314703343147033Human1name
127246453CV1075393single nucleotide variantNM_152419.3(HGSNAT):c.168A>G (p.Leu56=)Mucopolysaccharidosis, MPS-III-C [RCV001398972]likely benign84314699743146997Human1name
127244820CV1075394single nucleotide variantNM_152419.3(HGSNAT):c.294T>C (p.Ala98=)Mucopolysaccharidosis, MPS-III-C [RCV001393772]likely benign84315863443158634Human1name
127245581CV1097065single nucleotide variantNM_152419.3(HGSNAT):c.132A>G (p.Lys44=)Mucopolysaccharidosis, MPS-III-C [RCV001435239]likely benign84314696143146961Human1name
127284183CV1097066single nucleotide variantNM_152419.3(HGSNAT):c.210C>T (p.Tyr70=)Mucopolysaccharidosis, MPS-III-C [RCV001449060]likely benign84314703943147039Human1name
127333404CV1118613single nucleotide variantNM_152419.3(HGSNAT):c.144G>A (p.Glu48=)Mucopolysaccharidosis, MPS-III-C [RCV001472920]likely benign84314697343146973Human1name
127310260CV1118614single nucleotide variantNM_152419.3(HGSNAT):c.240G>A (p.Leu80=)Mucopolysaccharidosis, MPS-III-C [RCV001463818]likely benign84315858043158580Human1name
127311847CV1118615single nucleotide variantNM_152419.3(HGSNAT):c.249T>C (p.Val83=)Mucopolysaccharidosis, MPS-III-C [RCV001464239]likely benign84315858943158589Human1name
127299711CV1118616single nucleotide variantNM_152419.3(HGSNAT):c.258C>T (p.Asn86=)Mucopolysaccharidosis, MPS-III-C [RCV001478271]|Retinal dystrophy [RCV003888203]likely benign84315859843158598Human3name
127305507CV1118617single nucleotide variantNM_152419.3(HGSNAT):c.273A>G (p.Pro91=)Mucopolysaccharidosis, MPS-III-C [RCV001462499]likely benign84315861343158613Human1name
127336021CV1118618single nucleotide variantNM_152419.3(HGSNAT):c.282G>A (p.Gly94=)Mucopolysaccharidosis, MPS-III-C [RCV001474713]likely benign84315862243158622Human1name
150542457CV1314800duplicationNM_152419.3(HGSNAT):c.90dup (p.Arg31fs)Mucopolysaccharidosis, MPS-III-C [RCV003772151]|not provided [RCV001782251]pathogenic|likely pathogenic84314058243140583Human1name
151789612CV1397002single nucleotide variantNM_152419.3(HGSNAT):c.279A>G (p.Ala93=)Mucopolysaccharidosis, MPS-III-C [RCV001951922]likely benign84315861943158619Human1name
151814638CV1491341single nucleotide variantNM_152419.3(HGSNAT):c.195C>T (p.Thr65=)Mucopolysaccharidosis, MPS-III-C [RCV001975115]likely benign84314702443147024Human1name
151890058CV1514530single nucleotide variantNM_152419.3(HGSNAT):c.117A>C (p.Arg39=)Mucopolysaccharidosis, MPS-III-C [RCV001963554]uncertain significance84314061343140613Human1name
152071780CV1544039single nucleotide variantNM_152419.3(HGSNAT):c.183A>G (p.Glu61=)Mucopolysaccharidosis, MPS-III-C [RCV002169389]likely benign84314701243147012Human1name
152173834CV1567278single nucleotide variantNM_152419.3(HGSNAT):c.264T>C (p.Pro88=)Mucopolysaccharidosis, MPS-III-C [RCV002144243]likely benign84315860443158604Human1name
152116463CV1569585single nucleotide variantNM_152419.3(HGSNAT):c.261T>A (p.Val87=)Mucopolysaccharidosis, MPS-III-C [RCV002117256]likely benign84315860143158601Human1name
152147216CV1615602single nucleotide variantNM_152419.3(HGSNAT):c.291T>C (p.Ser97=)Mucopolysaccharidosis, MPS-III-C [RCV002101661]likely benign84315863143158631Human1name
152055969CV1662778single nucleotide variantNM_152419.3(HGSNAT):c.261T>C (p.Val87=)Mucopolysaccharidosis, MPS-III-C [RCV002146230]likely benign84315860143158601Human1name
156046091CV1868720single nucleotide variantNM_152419.3(HGSNAT):c.10G>C (p.Ala4Pro)Mucopolysaccharidosis, MPS-III-C [RCV003052831]benign84314050643140506Human1name
156381275CV1873650single nucleotide variantNM_152419.3(HGSNAT):c.171C>T (p.Leu57=)Mucopolysaccharidosis, MPS-III-C [RCV003067187]likely benign84314700043147000Human1name
156418846CV1918845single nucleotide variantNM_152419.3(HGSNAT):c.138T>C (p.His46=)Mucopolysaccharidosis, MPS-III-C [RCV002612056]likely benign84314696743146967Human1name
156446517CV1947862single nucleotide variantNM_152419.3(HGSNAT):c.180T>C (p.Asn60=)Mucopolysaccharidosis, MPS-III-C [RCV003118024]likely benign84314700943147009Human1name
156239066CV2047257single nucleotide variantNM_152419.3(HGSNAT):c.105C>G (p.Ala35=)Mucopolysaccharidosis, MPS-III-C [RCV002805608]likely benign84314060143140601Human1name
156315496CV2085997single nucleotide variantNM_152419.3(HGSNAT):c.105C>T (p.Ala35=)Mucopolysaccharidosis, MPS-III-C [RCV002898966]likely benign84314060143140601Human1name
156034936CV2123139single nucleotide variantNM_152419.3(HGSNAT):c.14G>T (p.Gly5Val)Inborn genetic diseases [RCV004068285]|Mucopolysaccharidosis, MPS-III-C [RCV002949389]uncertain significance84314051043140510Human2name
329953847CV2669184single nucleotide variantNM_152419.3(HGSNAT):c.20C>T (p.Ala7Val)not provided [RCV003231688]uncertain significance84314051643140516Humanname
405021797CV3088126single nucleotide variantNM_152419.3(HGSNAT):c.255A>G (p.Val85=)Mucopolysaccharidosis, MPS-III-C [RCV003795686]likely benign84315859543158595Human1name
11653638CV309247single nucleotide variantNM_152419.3(HGSNAT):c.111G>A (p.Pro37=)Mucopolysaccharidosis, MPS-III-C [RCV000312412]|Mucopolysaccharidosis, MPS-III-C [RCV002523684]likely benign|uncertain significance84314060743140607Human1name
405001463CV3095494single nucleotide variantNM_152419.3(HGSNAT):c.168A>T (p.Leu56=)Mucopolysaccharidosis, MPS-III-C [RCV003793797]likely benign84314699743146997Human1name
404978585CV3099063single nucleotide variantNM_152419.3(HGSNAT):c.102G>A (p.Gln34=)Mucopolysaccharidosis, MPS-III-C [RCV003791043]likely benign84314059843140598Human1name
405045229CV3103904single nucleotide variantNM_152419.3(HGSNAT):c.115C>A (p.Arg39=)Mucopolysaccharidosis, MPS-III-C [RCV003797622]likely benign84314061143140611Human1name
405081058CV3114860single nucleotide variantNM_152419.3(HGSNAT):c.186T>A (p.Leu62=)Mucopolysaccharidosis, MPS-III-C [RCV003810423]likely benign84314701543147015Human1name
11609607CV314589single nucleotide variantNM_152419.3(HGSNAT):c.17G>A (p.Arg6Lys)Inborn genetic diseases [RCV004022074]|Mucopolysaccharidosis, MPS-III-C [RCV000370676]|Mucopolysaccharidosis, MPS-III-C [RCV000907228]|Retinal dystrophy [RCV003889869]likely pathogenic|likely benign|uncertain significance84314051343140513Human4name
597652460CV3722779duplicationNM_152419.3(HGSNAT):c.61dup (p.Ala21fs)Mucopolysaccharidosis, MPS-III-C [RCV005041220]likely pathogenic84314055643140557Human1name
597735916CV3722780deletionNM_152419.3(HGSNAT):c.65del (p.Leu22fs)Mucopolysaccharidosis, MPS-III-C [RCV005051631]pathogenic|likely pathogenic84314056143140561Human1name
597922415CV3867292single nucleotide variantNM_152419.3(HGSNAT):c.189C>G (p.Leu63=)Mucopolysaccharidosis, MPS-III-C [RCV005223718]likely benign84314701843147018Human1name
14689760CV621282single nucleotide variantNM_152419.3(HGSNAT):c.204C>T (p.Thr68=)Mucopolysaccharidosis, MPS-III-C [RCV000972777]|not specified [RCV000780342]benign84314703343147033Human1name
15182841CV711544single nucleotide variantNM_152419.3(HGSNAT):c.199T>C (p.Leu67=)Mucopolysaccharidosis, MPS-III-C [RCV000974734]|Mucopolysaccharidosis, MPS-III-C [RCV001275624]likely benign|uncertain significance84314702843147028Human1name
15149889CV736686single nucleotide variantNM_152419.3(HGSNAT):c.285G>A (p.Lys95=)Mucopolysaccharidosis, MPS-III-C [RCV000901032]|Mucopolysaccharidosis, MPS-III-C [RCV001279457]likely benign84315862543158625Human1name
15187343CV766830single nucleotide variantNM_152419.3(HGSNAT):c.108G>C (p.Ala36=)Mucopolysaccharidosis, MPS-III-C [RCV001496756]likely benign84314060443140604Human1name
15142065CV766831single nucleotide variantNM_152419.3(HGSNAT):c.186T>C (p.Leu62=)Mucopolysaccharidosis, MPS-III-C [RCV000944011]likely benign84314701543147015Human1name
15101205CV783114single nucleotide variantNM_152419.3(HGSNAT):c.279A>C (p.Ala93=)Mucopolysaccharidosis, MPS-III-C [RCV001502427]likely benign84315861943158619Human1name
38487267CV934319single nucleotide variantNM_152419.3(HGSNAT):c.234C>T (p.His78=)Mucopolysaccharidosis, MPS-III-C [RCV001209242]|Mucopolysaccharidosis, MPS-III-C [RCV001828679]uncertain significance84314706343147063Human1name
126744587CV1028560single nucleotide variantNM_152419.3(HGSNAT):c.98C>T (p.Ala33Val)Mucopolysaccharidosis, MPS-III-C [RCV001351299]uncertain significance84314059443140594Human1name
127272540CV1061346duplicationNM_152419.3(HGSNAT):c.133dup (p.Arg45fs)Mucopolysaccharidosis, MPS-III-C [RCV001390498]pathogenic84314695543146956Human1name
127283469CV1075395single nucleotide variantNM_152419.3(HGSNAT):c.411C>G (p.Leu137=)Mucopolysaccharidosis, MPS-III-C [RCV001411839]likely benign84315896243158962Human1name
127275214CV1075396single nucleotide variantNM_152419.3(HGSNAT):c.411C>T (p.Leu137=)Mucopolysaccharidosis, MPS-III-C [RCV001406650]likely benign84315896243158962Human1name
127230098CV1075397single nucleotide variantNM_152419.3(HGSNAT):c.412T>C (p.Leu138=)Mucopolysaccharidosis, MPS-III-C [RCV001412346]likely benign84315896343158963Human1name
127250595CV1075399single nucleotide variantNM_152419.3(HGSNAT):c.558G>A (p.Leu186=)Mucopolysaccharidosis, MPS-III-C [RCV001399906]likely benign84316150243161502Human1name
127231829CV1075403single nucleotide variantNM_152419.3(HGSNAT):c.711G>A (p.Pro237=)Mucopolysaccharidosis, MPS-III-C [RCV001413232]likely benign84317066243170662Human1name
127282546CV1075404single nucleotide variantNM_152419.3(HGSNAT):c.720C>T (p.Leu240=)Mucopolysaccharidosis, MPS-III-C [RCV001411181]likely benign84317067143170671Human1name
127231989CV1075408single nucleotide variantNM_152419.3(HGSNAT):c.885A>G (p.Leu295=)Mucopolysaccharidosis, MPS-III-C [RCV001413276]|not provided [RCV004706120]likely benign84317810743178107Human1name
127282525CV1075409single nucleotide variantNM_152419.3(HGSNAT):c.951G>A (p.Arg317=)Mucopolysaccharidosis, MPS-III-C [RCV001411169]likely benign84317817343178173Human1name
127239225CV1097067single nucleotide variantNM_152419.3(HGSNAT):c.306T>C (p.Ser102=)Mucopolysaccharidosis, MPS-III-C [RCV001423083]likely benign84315864643158646Human1name
127274931CV1097068single nucleotide variantNM_152419.3(HGSNAT):c.339G>A (p.Leu113=)Mucopolysaccharidosis, MPS-III-C [RCV001443090]likely benign84315867943158679Human1name
127251247CV1097069single nucleotide variantNM_152419.3(HGSNAT):c.366T>G (p.Val122=)Mucopolysaccharidosis, MPS-III-C [RCV001425524]likely benign84315870643158706Human1name
127269380CV1097070single nucleotide variantNM_152419.3(HGSNAT):c.369T>C (p.Cys123=)Mucopolysaccharidosis, MPS-III-C [RCV001430262]likely benign84315870943158709Human1name
127276788CV1097071single nucleotide variantNM_152419.3(HGSNAT):c.483T>C (p.Asp161=)Mucopolysaccharidosis, MPS-III-C [RCV001432959]likely benign84315903443159034Human1name
127243784CV1097072single nucleotide variantNM_152419.3(HGSNAT):c.495T>C (p.Pro165=)Mucopolysaccharidosis, MPS-III-C [RCV001424015]likely benign84316143943161439Human1name
127267554CV1097075single nucleotide variantNM_152419.3(HGSNAT):c.690G>A (p.Thr230=)Mucopolysaccharidosis, MPS-III-C [RCV001429737]likely benign84317064143170641Human1name
127332159CV1118620single nucleotide variantNM_152419.3(HGSNAT):c.315C>T (p.Thr105=)Mucopolysaccharidosis, MPS-III-C [RCV001472065]likely benign84315865543158655Human1name
127300191CV1118622single nucleotide variantNM_152419.3(HGSNAT):c.405T>C (p.Tyr135=)Mucopolysaccharidosis, MPS-III-C [RCV001453798]likely benign84315895643158956Human1name
127290873CV1118623single nucleotide variantNM_152419.3(HGSNAT):c.708G>A (p.Leu236=)Mucopolysaccharidosis, MPS-III-C [RCV001451360]likely benign84317065943170659Human1name
127298818CV1118624single nucleotide variantNM_152419.3(HGSNAT):c.726C>T (p.Ser242=)Mucopolysaccharidosis, MPS-III-C [RCV001453443]likely benign84317067743170677Human1name
127290306CV1118627single nucleotide variantNM_152419.3(HGSNAT):c.849G>A (p.Pro283=)Mucopolysaccharidosis, MPS-III-C [RCV001458403]likely benign84317374143173741Human1name
127320474CV1118628single nucleotide variantNM_152419.3(HGSNAT):c.933G>T (p.Leu311=)Mucopolysaccharidosis, MPS-III-C [RCV001466924]likely benign84317815543178155Human1name
127314148CV1139497single nucleotide variantNM_152419.3(HGSNAT):c.453T>C (p.Cys151=)Mucopolysaccharidosis, MPS-III-C [RCV001502393]likely benign84315900443159004Human1name
127309194CV1139498single nucleotide variantNM_152419.3(HGSNAT):c.543C>T (p.Ser181=)Mucopolysaccharidosis, MPS-III-C [RCV001480778]likely benign84316148743161487Human1name
127310477CV1139499single nucleotide variantNM_152419.3(HGSNAT):c.559T>C (p.Leu187=)Mucopolysaccharidosis, MPS-III-C [RCV001481148]likely benign84316150343161503Human1name
127289082CV1139502single nucleotide variantNM_152419.3(HGSNAT):c.654G>A (p.Arg218=)Mucopolysaccharidosis, MPS-III-C [RCV001495514]likely benign84317060543170605Human1name
127329277CV1139503single nucleotide variantNM_152419.3(HGSNAT):c.672T>C (p.Gly224=)Mucopolysaccharidosis, MPS-III-C [RCV001487328]likely benign84317062343170623Human1name
127309971CV1139504single nucleotide variantNM_152419.3(HGSNAT):c.672T>G (p.Gly224=)Mucopolysaccharidosis, MPS-III-C [RCV001501199]likely benign84317062343170623Human1name
127326060CV1139505single nucleotide variantNM_152419.3(HGSNAT):c.675T>C (p.Asp225=)Mucopolysaccharidosis, MPS-III-C [RCV001485942]likely benign84317062643170626Human1name
127331327CV1139506single nucleotide variantNM_152419.3(HGSNAT):c.735C>G (p.Thr245=)Mucopolysaccharidosis, MPS-III-C [RCV001488721]likely benign84317068643170686Human1name
127318903CV1139508single nucleotide variantNM_152419.3(HGSNAT):c.768T>C (p.Phe256=)Mucopolysaccharidosis, MPS-III-C [RCV001503865]likely benign84317233443172334Human1name
127319350CV1139509single nucleotide variantNM_152419.3(HGSNAT):c.945A>G (p.Ala315=)Mucopolysaccharidosis, MPS-III-C [RCV001483829]likely benign84317816743178167Human1name
127332391CV1139510single nucleotide variantNM_152419.3(HGSNAT):c.987G>C (p.Val329=)Mucopolysaccharidosis, MPS-III-C [RCV001489459]likely benign84317820943178209Human1name
151854383CV1344336single nucleotide variantNM_152419.3(HGSNAT):c.777T>C (p.Tyr259=)Mucopolysaccharidosis, MPS-III-C [RCV001923210]likely benign84317234343172343Human1name
151724962CV1351025single nucleotide variantNM_152419.3(HGSNAT):c.74C>G (p.Pro25Arg)Mucopolysaccharidosis, MPS-III-C [RCV001891601]uncertain significance84314057043140570Human1name
151877709CV1361471single nucleotide variantNM_152419.3(HGSNAT):c.82T>C (p.Ser28Pro)Inborn genetic diseases [RCV004631820]|Mucopolysaccharidosis, MPS-III-C [RCV001926034]uncertain significance84314057843140578Human2name
151863697CV1374470single nucleotide variantNM_152419.3(HGSNAT):c.41C>T (p.Ala14Val)Mucopolysaccharidosis, MPS-III-C [RCV001884272]uncertain significance84314053743140537Human1name
151843566CV1499753single nucleotide variantNM_152419.3(HGSNAT):c.375G>A (p.Leu125=)Mucopolysaccharidosis, MPS-III-C [RCV001921826]uncertain significance84315892643158926Human1name
151796995CV1503769single nucleotide variantNM_152419.3(HGSNAT):c.89G>C (p.Gly30Ala)Mucopolysaccharidosis, MPS-III-C [RCV001973564]uncertain significance84314058543140585Human1name
152140757CV1520382single nucleotide variantNM_152419.3(HGSNAT):c.429T>C (p.His143=)Mucopolysaccharidosis, MPS-III-C [RCV002178028]likely benign84315898043158980Human1name
152126036CV1532429single nucleotide variantNM_152419.3(HGSNAT):c.345C>T (p.Asp115=)Mucopolysaccharidosis, MPS-III-C [RCV002118464]likely benign84315868543158685Human1name
152032732CV1537891single nucleotide variantNM_152419.3(HGSNAT):c.706C>T (p.Leu236=)Mucopolysaccharidosis, MPS-III-C [RCV002186952]likely benign84317065743170657Human1name
152052083CV1538923single nucleotide variantNM_152419.3(HGSNAT):c.331C>T (p.Leu111=)Mucopolysaccharidosis, MPS-III-C [RCV002189538]likely benign84315867143158671Human1name
152071164CV1570226single nucleotide variantNM_152419.3(HGSNAT):c.486T>C (p.Ser162=)Mucopolysaccharidosis, MPS-III-C [RCV002191802]likely benign84315903743159037Human1name
152155635CV1572898single nucleotide variantNM_152419.3(HGSNAT):c.651C>T (p.Ser217=)Mucopolysaccharidosis, MPS-III-C [RCV002180083]likely benign84317060243170602Human1name
152035373CV1583054single nucleotide variantNM_152419.3(HGSNAT):c.300T>C (p.Ala100=)Mucopolysaccharidosis, MPS-III-C [RCV002106894]likely benign84315864043158640Human1name
152082675CV1589621single nucleotide variantNM_152419.3(HGSNAT):c.468C>T (p.Asn156=)Mucopolysaccharidosis, MPS-III-C [RCV002112967]likely benign84315901943159019Human1name
152099152CV1595531single nucleotide variantNM_152419.3(HGSNAT):c.642A>T (p.Gly214=)Mucopolysaccharidosis, MPS-III-C [RCV002213770]likely benign84317059343170593Human1name
152076917CV1607105single nucleotide variantNM_152419.3(HGSNAT):c.570T>C (p.Asp190=)Mucopolysaccharidosis, MPS-III-C [RCV002130345]likely benign84316917943169179Human1name
152043369CV1618201single nucleotide variantNM_152419.3(HGSNAT):c.912G>T (p.Gly304=)Mucopolysaccharidosis, MPS-III-C [RCV002206636]likely benign84317813443178134Human1name
152085736CV1621079single nucleotide variantNM_152419.3(HGSNAT):c.600A>C (p.Ile200=)Mucopolysaccharidosis, MPS-III-C [RCV002193608]likely benign84316920943169209Human1name
152071835CV1633851single nucleotide variantNM_152419.3(HGSNAT):c.360A>G (p.Lys120=)Mucopolysaccharidosis, MPS-III-C [RCV002191884]likely benign84315870043158700Human1name
152055094CV1648695single nucleotide variantNM_152419.3(HGSNAT):c.699A>C (p.Leu233=)Mucopolysaccharidosis, MPS-III-C [RCV002072833]likely benign84317065043170650Human1name
152058108CV1651960single nucleotide variantNM_152419.3(HGSNAT):c.714C>G (p.Pro238=)Mucopolysaccharidosis, MPS-III-C [RCV002190209]likely benign84317066543170665Human1name
152088935CV1655784single nucleotide variantNM_152419.3(HGSNAT):c.417A>G (p.Val139=)Mucopolysaccharidosis, MPS-III-C [RCV002194039]likely benign84315896843158968Human1name
152025987CV1666146single nucleotide variantNM_152419.3(HGSNAT):c.996T>C (p.Asn332=)Mucopolysaccharidosis, MPS-III-C [RCV002084649]likely benign84317821843178218Human1name
156358135CV1904054single nucleotide variantNM_152419.3(HGSNAT):c.64C>G (p.Leu22Val)Mucopolysaccharidosis, MPS-III-C [RCV002581534]uncertain significance84314056043140560Human1name
156134354CV1914483single nucleotide variantNM_152419.3(HGSNAT):c.936G>T (p.Gly312=)Mucopolysaccharidosis, MPS-III-C [RCV002623431]uncertain significance84317815843178158Human1name
156218143CV1927987single nucleotide variantNM_152419.3(HGSNAT):c.423C>T (p.Asn141=)Mucopolysaccharidosis, MPS-III-C [RCV002644288]likely benign84315897443158974Human1name
156446917CV1948603single nucleotide variantNM_152419.3(HGSNAT):c.28G>C (p.Ala10Pro)Inborn genetic diseases [RCV004244646]|Mucopolysaccharidosis, MPS-III-C [RCV003118438]uncertain significance84314052443140524Human2name
156400242CV1982231single nucleotide variantNM_152419.3(HGSNAT):c.96T>A (p.Asp32Glu)Mucopolysaccharidosis, MPS-III-C [RCV002635900]uncertain significance84314059243140592Human1name
156345567CV1995172single nucleotide variantNM_152419.3(HGSNAT):c.582T>C (p.Asn194=)Mucopolysaccharidosis, MPS-III-C [RCV002650554]likely benign84316919143169191Human1name
156184653CV2020622single nucleotide variantNM_152419.3(HGSNAT):c.807T>C (p.His269=)Mucopolysaccharidosis, MPS-III-C [RCV002710891]likely benign84317237343172373Human1name
156052418CV2027407single nucleotide variantNM_152419.3(HGSNAT):c.918A>G (p.Ser306=)Mucopolysaccharidosis, MPS-III-C [RCV002736554]likely benign84317814043178140Human1name
156144706CV2033105single nucleotide variantNM_152419.3(HGSNAT):c.52C>G (p.Leu18Val)Mucopolysaccharidosis, MPS-III-C [RCV002741023]uncertain significance84314054843140548Human1name
156189156CV2052303single nucleotide variantNM_152419.3(HGSNAT):c.357G>A (p.Glu119=)Mucopolysaccharidosis, MPS-III-C [RCV002828554]likely benign84315869743158697Human1name
156014549CV2061532single nucleotide variantNM_152419.3(HGSNAT):c.420G>A (p.Lys140=)Mucopolysaccharidosis, MPS-III-C [RCV002820304]likely benign84315897143158971Human1name
156213856CV2074391single nucleotide variantNM_152419.3(HGSNAT):c.750T>C (p.Ala250=)Mucopolysaccharidosis, MPS-III-C [RCV002829408]likely benign84317231643172316Human1name
155937346CV2075016single nucleotide variantNM_152419.3(HGSNAT):c.624C>T (p.Leu208=)Mucopolysaccharidosis, MPS-III-C [RCV002861537]likely benign84316923343169233Human1name
156203685CV2076599single nucleotide variantNM_152419.3(HGSNAT):c.792T>C (p.Tyr264=)Mucopolysaccharidosis, MPS-III-C [RCV002852557]likely benign84317235843172358Human1name
155901879CV2083866single nucleotide variantNM_152419.3(HGSNAT):c.681G>A (p.Gln227=)Mucopolysaccharidosis, MPS-III-C [RCV002857910]likely benign84317063243170632Human1name
156233209CV2093916single nucleotide variantNM_152419.3(HGSNAT):c.999T>C (p.Tyr333=)Mucopolysaccharidosis, MPS-III-C [RCV002894632]likely benign84317822143178221Human1name
155927688CV2145231single nucleotide variantNM_152419.3(HGSNAT):c.547C>T (p.Leu183=)Mucopolysaccharidosis, MPS-III-C [RCV003013487]likely benign84316149143161491Human1name
156239570CV2152278single nucleotide variantNM_152419.3(HGSNAT):c.621C>T (p.Arg207=)Mucopolysaccharidosis, MPS-III-C [RCV003008049]likely benign84316923043169230Human1name
405022578CV3081842single nucleotide variantNM_152419.3(HGSNAT):c.888G>C (p.Ser296=)Mucopolysaccharidosis, MPS-III-C [RCV003785448]likely benign84317811043178110Human1name
404988291CV3084002single nucleotide variantNM_152419.3(HGSNAT):c.909G>A (p.Arg303=)Mucopolysaccharidosis, MPS-III-C [RCV003782194]likely benign84317813143178131Human1name
405047631CV3084416single nucleotide variantNM_152419.3(HGSNAT):c.738C>T (p.Phe246=)Mucopolysaccharidosis, MPS-III-C [RCV003797823]likely benign84317068943170689Human1name
405023310CV3084954single nucleotide variantNM_152419.3(HGSNAT):c.705C>T (p.Ala235=)Mucopolysaccharidosis, MPS-III-C [RCV003795820]likely benign84317065643170656Human1name
402504299CV3088723single nucleotide variantNM_152419.3(HGSNAT):c.657A>G (p.Thr219=)Mucopolysaccharidosis, MPS-III-C [RCV003779432]likely benign84317060843170608Human1name
405012739CV3093498single nucleotide variantNM_152419.3(HGSNAT):c.378A>G (p.Glu126=)Mucopolysaccharidosis, MPS-III-C [RCV003784502]likely benign84315892943158929Human1name
405046326CV3097317single nucleotide variantNM_152419.3(HGSNAT):c.86C>A (p.Ser29Ter)Mucopolysaccharidosis, MPS-III-C [RCV003807897]pathogenic84314058243140582Human1name
404978613CV3099070single nucleotide variantNM_152419.3(HGSNAT):c.823C>T (p.Leu275=)Mucopolysaccharidosis, MPS-III-C [RCV003791050]likely benign84317371543173715Human1name
405072386CV3099902single nucleotide variantNM_152419.3(HGSNAT):c.408T>C (p.Ser136=)Mucopolysaccharidosis, MPS-III-C [RCV003799617]likely benign84315895943158959Human1name
405001708CV3102004single nucleotide variantNM_152419.3(HGSNAT):c.705C>G (p.Ala235=)Mucopolysaccharidosis, MPS-III-C [RCV003804049]likely benign84317065643170656Human1name
405005027CV3102303single nucleotide variantNM_152419.3(HGSNAT):c.402C>T (p.Asn134=)Mucopolysaccharidosis, MPS-III-C [RCV003804349]likely benign84315895343158953Human1name
405008875CV3105952single nucleotide variantNM_152419.3(HGSNAT):c.579C>T (p.Asn193=)Mucopolysaccharidosis, MPS-III-C [RCV003794450]likely benign84316918843169188Human1name
405037488CV3106300single nucleotide variantNM_152419.3(HGSNAT):c.510C>T (p.Phe170=)Mucopolysaccharidosis, MPS-III-C [RCV003796991]likely benign84316145443161454Human1name
405087709CV3108039single nucleotide variantNM_152419.3(HGSNAT):c.618T>C (p.Asp206=)Mucopolysaccharidosis, MPS-III-C [RCV003800737]likely benign84316922743169227Human1name
405058115CV3108218single nucleotide variantNM_152419.3(HGSNAT):c.552G>A (p.Arg184=)Mucopolysaccharidosis, MPS-III-C [RCV003808796]likely benign84316149643161496Human1name
405009591CV3109080single nucleotide variantNM_152419.3(HGSNAT):c.435A>G (p.Gly145=)Mucopolysaccharidosis, MPS-III-C [RCV003804747]likely benign84315898643158986Human1name
405157076CV3109393single nucleotide variantNM_152419.3(HGSNAT):c.771C>T (p.Val257=)Mucopolysaccharidosis, MPS-III-C [RCV003801917]likely benign84317233743172337Human1name
405124926CV3111808single nucleotide variantNM_152419.3(HGSNAT):c.945A>T (p.Ala315=)Mucopolysaccharidosis, MPS-III-C [RCV003815281]likely benign84317816743178167Human1name
405082536CV3113522single nucleotide variantNM_152419.3(HGSNAT):c.333G>T (p.Leu111=)Mucopolysaccharidosis, MPS-III-C [RCV003810539]likely benign84315867343158673Human1name
11609770CV314595single nucleotide variantNM_152419.3(HGSNAT):c.342C>T (p.Asn114=)Mucopolysaccharidosis, MPS-III-C [RCV000372738]|Mucopolysaccharidosis, MPS-III-C [RCV001083633]|not provided [RCV000675863]|not specified [RCV002222495]likely benign|uncertain significance84315868243158682Human1name
405262820CV3188377single nucleotide variantNM_152419.3(HGSNAT):c.636G>A (p.Glu212=)Retinal dystrophy [RCV003889441]uncertain significance84317058743170587Human2name
407521926CV3437249single nucleotide variantNM_152419.3(HGSNAT):c.86C>G (p.Ser29Trp)Inborn genetic diseases [RCV004630557]uncertain significance84314058243140582Human1name
597652478CV3722782duplicationNM_152419.3(HGSNAT):c.208dup (p.Tyr70fs)Mucopolysaccharidosis, MPS-III-C [RCV005041222]likely pathogenic84314703643147037Human1name
597854659CV3870515single nucleotide variantNM_152419.3(HGSNAT):c.71C>T (p.Ala24Val)Mucopolysaccharidosis, MPS-III-C [RCV005228716]likely benign84314056743140567Human1name
597875856CV3871390single nucleotide variantNM_152419.3(HGSNAT):c.318G>A (p.Gln106=)Mucopolysaccharidosis, MPS-III-C [RCV005216604]likely benign84315865843158658Human1name
597900873CV3876573single nucleotide variantNM_152419.3(HGSNAT):c.315C>G (p.Thr105=)Mucopolysaccharidosis, MPS-III-C [RCV005220271]likely benign84315865543158655Human1name
13808565CV565143single nucleotide variantNM_152419.3(HGSNAT):c.89G>A (p.Gly30Glu)Mucopolysaccharidosis, MPS-III-C [RCV000701728]|Mucopolysaccharidosis, MPS-III-C [RCV001825380]uncertain significance84314058543140585Human1name
15141374CV711546single nucleotide variantNM_152419.3(HGSNAT):c.765C>T (p.Val255=)Mucopolysaccharidosis, MPS-III-C [RCV000966296]|Mucopolysaccharidosis, MPS-III-C [RCV001275628]likely benign|uncertain significance84317233143172331Human1name
15177414CV711547single nucleotide variantNM_152419.3(HGSNAT):c.888G>A (p.Ser296=)Mucopolysaccharidosis, MPS-III-C [RCV000973420]|Mucopolysaccharidosis, MPS-III-C [RCV001827060]likely benign84317811043178110Human1name
15189697CV723111single nucleotide variantNM_152419.3(HGSNAT):c.928T>C (p.Leu310=)Mucopolysaccharidosis, MPS-III-C [RCV000887893]|Mucopolysaccharidosis, MPS-III-C [RCV001830944]likely benign84317815043178150Human1name
15150536CV736687single nucleotide variantNM_152419.3(HGSNAT):c.741G>A (p.Arg247=)Mucopolysaccharidosis, MPS-III-C [RCV000901175]|Mucopolysaccharidosis, MPS-III-C [RCV001159325]likely benign|uncertain significance84317069243170692Human1name
15194654CV751172single nucleotide variantNM_152419.3(HGSNAT):c.321C>T (p.His107=)Mucopolysaccharidosis, MPS-III-C [RCV000911186]likely benign84315866143158661Human1name
15168629CV751173single nucleotide variantNM_152419.3(HGSNAT):c.652A>C (p.Arg218=)Mucopolysaccharidosis, MPS-III-C [RCV000927332]likely benign84317060343170603Human1name
15118406CV751175single nucleotide variantNM_152419.3(HGSNAT):c.699A>G (p.Leu233=)Mucopolysaccharidosis, MPS-III-C [RCV000917969]likely benign84317065043170650Human1name
15176220CV766833single nucleotide variantNM_152419.3(HGSNAT):c.576T>C (p.Phe192=)Mucopolysaccharidosis, MPS-III-C [RCV001456484]likely benign84316918543169185Human1name
15114766CV783115single nucleotide variantNM_152419.3(HGSNAT):c.837C>T (p.Asp279=)Mucopolysaccharidosis, MPS-III-C [RCV001477393]likely benign84317372943173729Human1name
28872070CV899649single nucleotide variantNM_152419.3(HGSNAT):c.591T>C (p.Ser197=)Mucopolysaccharidosis, MPS-III-C [RCV001164230]|Mucopolysaccharidosis, MPS-III-C [RCV001492187]likely benign|uncertain significance84316920043169200Human1name
38460197CV919158deletionNM_152419.3(HGSNAT):c.272del (p.Pro91fs)Mucopolysaccharidosis, MPS-III-C [RCV005049784]|Retinitis pigmentosa 73 [RCV001196380]likely pathogenic84315861143158611Human2name
38456331CV934318deletionNM_152419.3(HGSNAT):c.150del (p.Met51fs)Mucopolysaccharidosis, MPS-III-C [RCV001210786]pathogenic84314697943146979Human1name
38473923CV946077deletionNM_152419.3(HGSNAT):c.111del (p.Pro38fs)Mucopolysaccharidosis, MPS-III-C [RCV001232001]pathogenic84314060743140607Human1name
126753323CV1008044single nucleotide variantNM_152419.3(HGSNAT):c.110C>T (p.Pro37Leu)Mucopolysaccharidosis, MPS-III-C [RCV001327263]|Mucopolysaccharidosis, MPS-III-C [RCV001831030]uncertain significance84314060643140606Human1name
8643414CV102397single nucleotide variantNM_152419.3(HGSNAT):c.1749T>C (p.Tyr583=)Mucopolysaccharidosis, MPS-III-C [RCV000610663]|Mucopolysaccharidosis, MPS-III-C [RCV001518419]|Retinitis pigmentosa 73 [RCV001532826]|not provided [RCV000588987]|not specified [RCV000082655]benign84319941043199410Human2name
126764731CV1028564single nucleotide variantNM_152419.3(HGSNAT):c.1128G>T (p.Ser376=)Mucopolysaccharidosis, MPS-III-C [RCV001341765]|Mucopolysaccharidosis, MPS-III-C [RCV001831075]|Retinal dystrophy [RCV004815405]uncertain significance84318226043182260Human3name
126725731CV1028566single nucleotide variantNM_152419.3(HGSNAT):c.1392C>A (p.Thr464=)Mucopolysaccharidosis, MPS-III-C [RCV001348240]likely benign|uncertain significance84319377143193771Human1name
126912366CV1037869single nucleotide variantNM_152419.3(HGSNAT):c.137A>T (p.His46Leu)Mucopolysaccharidosis, MPS-III-C [RCV003771043]|not provided [RCV001356453]uncertain significance84314696643146966Human1name
126919932CV1045534single nucleotide variantNM_152419.3(HGSNAT):c.278C>G (p.Ala93Gly)Mucopolysaccharidosis, MPS-III-C [RCV001373512]uncertain significance84315861843158618Human1name
127283187CV1075410single nucleotide variantNM_152419.3(HGSNAT):c.1182G>C (p.Leu394=)Mucopolysaccharidosis, MPS-III-C [RCV001411602]likely benign84319152743191527Human1name
127282129CV1075412single nucleotide variantNM_152419.3(HGSNAT):c.1401C>T (p.Ala467=)Mucopolysaccharidosis, MPS-III-C [RCV001410930]likely benign84319378043193780Human1name
127274884CV1075413single nucleotide variantNM_152419.3(HGSNAT):c.1440C>T (p.Ile480=)Mucopolysaccharidosis, MPS-III-C [RCV001406511]likely benign84319381943193819Human1name
127258528CV1075415single nucleotide variantNM_152419.3(HGSNAT):c.1521C>T (p.Phe507=)Mucopolysaccharidosis, MPS-III-C [RCV001401705]likely benign84319700443197004Human1name
127267658CV1075417single nucleotide variantNM_152419.3(HGSNAT):c.1617C>G (p.Ser539=)Mucopolysaccharidosis, MPS-III-C [RCV001404171]likely benign84319784343197843Human1name
127234871CV1075418single nucleotide variantNM_152419.3(HGSNAT):c.1680T>G (p.Val560=)Mucopolysaccharidosis, MPS-III-C [RCV001396511]likely benign84319790643197906Human1name
127253766CV1075419single nucleotide variantNM_152419.3(HGSNAT):c.1698G>A (p.Leu566=)Mucopolysaccharidosis, MPS-III-C [RCV001400639]likely benign84319792443197924Human1name
127229962CV1075420single nucleotide variantNM_152419.3(HGSNAT):c.1815C>T (p.His605=)Mucopolysaccharidosis, MPS-III-C [RCV001412254]likely benign84319947643199476Human1name
127269527CV1075421single nucleotide variantNM_152419.3(HGSNAT):c.1821G>A (p.Glu607=)Mucopolysaccharidosis, MPS-III-C [RCV001404736]likely benign84319948243199482Human1name
127241552CV1075422single nucleotide variantNM_152419.3(HGSNAT):c.1836C>T (p.Asn612=)Mucopolysaccharidosis, MPS-III-C [RCV001398009]|Mucopolysaccharidosis, MPS-III-C [RCV001826195]likely benign84319949743199497Human1name
127276999CV1075423single nucleotide variantNM_152419.3(HGSNAT):c.1872C>T (p.Tyr624=)Mucopolysaccharidosis, MPS-III-C [RCV001407500]likely benign84319953343199533Human1name
127279559CV1097077single nucleotide variantNM_152419.3(HGSNAT):c.1125C>T (p.Ala375=)Mucopolysaccharidosis, MPS-III-C [RCV001445869]likely benign84318225743182257Human1name
127278516CV1097079single nucleotide variantNM_152419.3(HGSNAT):c.1191G>C (p.Leu397=)Mucopolysaccharidosis, MPS-III-C [RCV001445119]likely benign84319153643191536Human1name
127277952CV1097080single nucleotide variantNM_152419.3(HGSNAT):c.1302C>T (p.Cys434=)Mucopolysaccharidosis, MPS-III-C [RCV001444701]likely benign84319235543192355Human1name
127276489CV1097081single nucleotide variantNM_152419.3(HGSNAT):c.1326C>T (p.Ile442=)Mucopolysaccharidosis, MPS-III-C [RCV001432839]likely benign84319237943192379Human1name
127281411CV1097082single nucleotide variantNM_152419.3(HGSNAT):c.1338G>C (p.Leu446=)Mucopolysaccharidosis, MPS-III-C [RCV001447146]likely benign84319239143192391Human1name
127236150CV1097083single nucleotide variantNM_152419.3(HGSNAT):c.1359C>T (p.Tyr453=)Mucopolysaccharidosis, MPS-III-C [RCV001433286]likely benign84319241243192412Human1name
127278567CV1097084single nucleotide variantNM_152419.3(HGSNAT):c.1371T>A (p.Ser457=)Mucopolysaccharidosis, MPS-III-C [RCV001445148]likely benign84319242443192424Human1name
127258965CV1097088single nucleotide variantNM_152419.3(HGSNAT):c.1629C>T (p.Val543=)Mucopolysaccharidosis, MPS-III-C [RCV001438267]likely benign84319785543197855Human1name
127272056CV1097089single nucleotide variantNM_152419.3(HGSNAT):c.1704A>G (p.Thr568=)Mucopolysaccharidosis, MPS-III-C [RCV001431176]likely benign84319793043197930Human1name
127237498CV1097090single nucleotide variantNM_152419.3(HGSNAT):c.1755C>T (p.Gly585=)Mucopolysaccharidosis, MPS-III-C [RCV001422711]likely benign84319941643199416Human1name
127270992CV1097091single nucleotide variantNM_152419.3(HGSNAT):c.1803C>T (p.Asp601=)Mucopolysaccharidosis, MPS-III-C [RCV001430794]likely benign84319946443199464Human1name
127327553CV1118630single nucleotide variantNM_152419.3(HGSNAT):c.1107T>C (p.Pro369=)Mucopolysaccharidosis, MPS-III-C [RCV001469127]likely benign84318223943182239Human1name
127294371CV1118631single nucleotide variantNM_152419.3(HGSNAT):c.1125C>G (p.Ala375=)Mucopolysaccharidosis, MPS-III-C [RCV001452226]likely benign84318225743182257Human1name
127324500CV1118632single nucleotide variantNM_152419.3(HGSNAT):c.1224C>T (p.Phe408=)Mucopolysaccharidosis, MPS-III-C [RCV001468218]likely benign84319156943191569Human1name
127309561CV1118634single nucleotide variantNM_152419.3(HGSNAT):c.1477C>T (p.Leu493=)Mucopolysaccharidosis, MPS-III-C [RCV001463660]likely benign84319696043196960Human1name
127299690CV1118636single nucleotide variantNM_152419.3(HGSNAT):c.1545G>A (p.Gly515=)Mucopolysaccharidosis, MPS-III-C [RCV001460893]likely benign84319767443197674Human1name
127318955CV1118637single nucleotide variantNM_152419.3(HGSNAT):c.1632T>C (p.Thr544=)Mucopolysaccharidosis, MPS-III-C [RCV001466410]likely benign84319785843197858Human1name
127330933CV1118638single nucleotide variantNM_152419.3(HGSNAT):c.1779C>T (p.Phe593=)Mucopolysaccharidosis, MPS-III-C [RCV001471246]likely benign84319944043199440Human1name
127298942CV1118639single nucleotide variantNM_152419.3(HGSNAT):c.1842C>A (p.Val614=)Mucopolysaccharidosis, MPS-III-C [RCV001460673]likely benign84319950343199503Human1name
127291323CV1118640single nucleotide variantNM_152419.3(HGSNAT):c.1842C>T (p.Val614=)Mucopolysaccharidosis, MPS-III-C [RCV001476038]|not provided [RCV003426133]likely benign84319950343199503Human1name
127318255CV1139511single nucleotide variantNM_152419.3(HGSNAT):c.1002C>T (p.Cys334=)Mucopolysaccharidosis, MPS-III-C [RCV001483469]likely benign84317822443178224Human1name
127328920CV1139512single nucleotide variantNM_152419.3(HGSNAT):c.1044G>A (p.Val348=)Mucopolysaccharidosis, MPS-III-C [RCV001487071]likely benign84318217643182176Human1name
127316931CV1139513single nucleotide variantNM_152419.3(HGSNAT):c.1116A>G (p.Glu372=)Mucopolysaccharidosis, MPS-III-C [RCV001483016]likely benign84318224843182248Human1name
127315704CV1139514single nucleotide variantNM_152419.3(HGSNAT):c.1290G>A (p.Lys430=)Mucopolysaccharidosis, MPS-III-C [RCV001482587]likely benign84319234343192343Human1name
127305130CV1139515single nucleotide variantNM_152419.3(HGSNAT):c.1479A>G (p.Leu493=)Mucopolysaccharidosis, MPS-III-C [RCV001479714]likely benign84319696243196962Human1name
127316513CV1139517single nucleotide variantNM_152419.3(HGSNAT):c.1839C>T (p.Ile613=)Mucopolysaccharidosis, MPS-III-C [RCV001482883]|Mucopolysaccharidosis, MPS-III-C [RCV001832629]|Retinal dystrophy [RCV003888209]|not provided [RCV001581157]likely benign84319950043199500Human3name
127318091CV1139518single nucleotide variantNM_152419.3(HGSNAT):c.1845C>T (p.Ala615=)Mucopolysaccharidosis, MPS-III-C [RCV001503562]likely benign84319950643199506Human1name
127327395CV1139519single nucleotide variantNM_152419.3(HGSNAT):c.1907G>A (p.Ter636=)Mucopolysaccharidosis, MPS-III-C [RCV001486343]likely benign84319956843199568Human1name
150336767CV1165878single nucleotide variantNM_152419.3(HGSNAT):c.1758C>T (p.His586=)Mucopolysaccharidosis, MPS-III-C [RCV002070387]|not provided [RCV001532140]likely benign84319941943199419Human1name
150429540CV1189320single nucleotide variantNM_152419.3(HGSNAT):c.1269G>A (p.Gly423=)Mucopolysaccharidosis, MPS-III-C [RCV001563770]|Mucopolysaccharidosis, MPS-III-C [RCV002070393]|Retinitis pigmentosa 73 [RCV001563771]likely benign|uncertain significance84319232243192322Human2name
151824276CV1350856single nucleotide variantNM_152419.3(HGSNAT):c.185T>C (p.Leu62Pro)Mucopolysaccharidosis, MPS-III-C [RCV001919872]uncertain significance84314701443147014Human1name
151817509CV1385623single nucleotide variantNM_152419.3(HGSNAT):c.278C>T (p.Ala93Val)Inborn genetic diseases [RCV005350849]|Mucopolysaccharidosis, MPS-III-C [RCV002013048]uncertain significance84315861843158618Human2name
151859390CV1403705single nucleotide variantNM_152419.3(HGSNAT):c.174C>G (p.Ile58Met)Mucopolysaccharidosis, MPS-III-C [RCV001996935]uncertain significance84314700343147003Human1name
151720988CV1420944deletionNM_152419.3(HGSNAT):c.719del (p.Leu240fs)Mucopolysaccharidosis, MPS-III-C [RCV002040075]pathogenic84317067043170670Human1name
151866734CV1446473single nucleotide variantNM_152419.3(HGSNAT):c.260T>G (p.Val87Gly)Mucopolysaccharidosis, MPS-III-C [RCV001980805]uncertain significance84315860043158600Human1name
151792083CV1471045single nucleotide variantNM_152419.3(HGSNAT):c.110C>G (p.Pro37Arg)Mucopolysaccharidosis, MPS-III-C [RCV001931515]uncertain significance84314060643140606Human1name
151773196CV1504772single nucleotide variantNM_152419.3(HGSNAT):c.142G>A (p.Glu48Lys)Mucopolysaccharidosis, MPS-III-C [RCV002009043]uncertain significance84314697143146971Human1name
152044899CV1525642single nucleotide variantNM_152419.3(HGSNAT):c.1368A>G (p.Pro456=)Mucopolysaccharidosis, MPS-III-C [RCV002126544]likely benign84319242143192421Human1name
152144647CV1543160single nucleotide variantNM_152419.3(HGSNAT):c.1227C>T (p.Leu409=)Mucopolysaccharidosis, MPS-III-C [RCV002178534]likely benign84319157243191572Human1name
152082546CV1558847single nucleotide variantNM_152419.3(HGSNAT):c.1669C>T (p.Leu557=)Mucopolysaccharidosis, MPS-III-C [RCV002149501]likely benign84319789543197895Human1name
152138818CV1563571single nucleotide variantNM_152419.3(HGSNAT):c.1392C>G (p.Thr464=)Mucopolysaccharidosis, MPS-III-C [RCV002200309]likely benign84319377143193771Human1name
152092660CV1567821single nucleotide variantNM_152419.3(HGSNAT):c.1230G>T (p.Leu410=)Mucopolysaccharidosis, MPS-III-C [RCV002212943]likely benign84319157543191575Human1name
152111242CV1582296single nucleotide variantNM_152419.3(HGSNAT):c.1155C>T (p.Asp385=)Mucopolysaccharidosis, MPS-III-C [RCV002080278]likely benign84319150043191500Human1name
152144477CV1582525single nucleotide variantNM_152419.3(HGSNAT):c.1824C>T (p.His608=)Mucopolysaccharidosis, MPS-III-C [RCV002201026]likely benign84319948543199485Human1name
152132154CV1585034single nucleotide variantNM_152419.3(HGSNAT):c.1638C>A (p.Leu546=)Mucopolysaccharidosis, MPS-III-C [RCV002083008]likely benign84319786443197864Human1name
152025936CV1586636single nucleotide variantNM_152419.3(HGSNAT):c.1008T>A (p.Gly336=)Mucopolysaccharidosis, MPS-III-C [RCV002184987]likely benign84317823043178230Human1name
152136236CV1587814single nucleotide variantNM_152419.3(HGSNAT):c.1045C>T (p.Leu349=)Mucopolysaccharidosis, MPS-III-C [RCV002083541]likely benign84318217743182177Human1name
152035996CV1590541single nucleotide variantNM_152419.3(HGSNAT):c.1635G>C (p.Thr545=)Mucopolysaccharidosis, MPS-III-C [RCV002205584]likely benign84319786143197861Human1name
152155712CV1620577single nucleotide variantNM_152419.3(HGSNAT):c.1671G>A (p.Leu557=)Mucopolysaccharidosis, MPS-III-C [RCV002122384]likely benign84319789743197897Human1name
152044406CV1622004single nucleotide variantNM_152419.3(HGSNAT):c.1161G>A (p.Thr387=)Mucopolysaccharidosis, MPS-III-C [RCV002108162]likely benign84319150643191506Human1name
152107699CV1624087single nucleotide variantNM_152419.3(HGSNAT):c.1677A>G (p.Pro559=)Mucopolysaccharidosis, MPS-III-C [RCV002134073]likely benign84319790343197903Human1name
8595353CV16274duplicationNM_152419.3(HGSNAT):c.525dup (p.Val176fs)Mucopolysaccharidosis, MPS-III-C [RCV000001294]|Mucopolysaccharidosis, MPS-III-C [RCV002476908]|not provided [RCV002243612]pathogenic84316146843161469Human1name
152176485CV1631422single nucleotide variantNM_152419.3(HGSNAT):c.1299T>C (p.Asn433=)Mucopolysaccharidosis, MPS-III-C [RCV002164630]likely benign84319235243192352Human1name
152151724CV1631583single nucleotide variantNM_152419.3(HGSNAT):c.1050G>A (p.Gln350=)Mucopolysaccharidosis, MPS-III-C [RCV002179556]likely benign84318218243182182Human1name
152150421CV1636263single nucleotide variantNM_152419.3(HGSNAT):c.1710C>T (p.Thr570=)Mucopolysaccharidosis, MPS-III-C [RCV002102143]likely benign84319793643197936Human1name
152086158CV1645315single nucleotide variantNM_152419.3(HGSNAT):c.1473A>G (p.Lys491=)Mucopolysaccharidosis, MPS-III-C [RCV002131453]likely benign84319695643196956Human1name
152084849CV1646483single nucleotide variantNM_152419.3(HGSNAT):c.1173C>T (p.Pro391=)Mucopolysaccharidosis, MPS-III-C [RCV002149789]likely benign84319151843191518Human1name
152060323CV1648669single nucleotide variantNM_152419.3(HGSNAT):c.1161G>T (p.Thr387=)Mucopolysaccharidosis, MPS-III-C [RCV002090175]likely benign84319150643191506Human1name
152165467CV1649260single nucleotide variantNM_152419.3(HGSNAT):c.1557T>C (p.Val519=)Mucopolysaccharidosis, MPS-III-C [RCV002204251]likely benign84319768643197686Human1name
152147926CV1656279single nucleotide variantNM_152419.3(HGSNAT):c.1764G>A (p.Val588=)Mucopolysaccharidosis, MPS-III-C [RCV002220340]likely benign84319942543199425Human1name
152073905CV1660520single nucleotide variantNM_152419.3(HGSNAT):c.1710C>A (p.Thr570=)Mucopolysaccharidosis, MPS-III-C [RCV002169648]likely benign84319793643197936Human1name
155726012CV1783691duplicationNM_152419.3(HGSNAT):c.728dup (p.Asp244fs)Mucopolysaccharidosis, MPS-III-C [RCV002307135]likely pathogenic84317067843170679Human1name
156249543CV1886926single nucleotide variantNM_152419.3(HGSNAT):c.1281T>C (p.Asp427=)Mucopolysaccharidosis, MPS-III-C [RCV003086053]likely benign84319233443192334Human1name
155969609CV1888868single nucleotide variantNM_152419.3(HGSNAT):c.239T>C (p.Leu80Ser)Mucopolysaccharidosis, MPS-III-C [RCV003075112]uncertain significance84315857943158579Human1name
156344090CV1907572single nucleotide variantNM_152419.3(HGSNAT):c.263C>T (p.Pro88Leu)Mucopolysaccharidosis, MPS-III-C [RCV003090534]uncertain significance84315860343158603Human1name
156047987CV1914912single nucleotide variantNM_152419.3(HGSNAT):c.253G>A (p.Val85Ile)Mucopolysaccharidosis, MPS-III-C [RCV002620505]uncertain significance84315859343158593Human1name
156087438CV1919578single nucleotide variantNM_152419.3(HGSNAT):c.1713A>T (p.Pro571=)Mucopolysaccharidosis, MPS-III-C [RCV002591787]likely benign84319793943197939Human1name
156081916CV1972141single nucleotide variantNM_152419.3(HGSNAT):c.1065A>T (p.Thr355=)Mucopolysaccharidosis, MPS-III-C [RCV002621572]likely benign84318219743182197Human1name
156393636CV1983445single nucleotide variantNM_152419.3(HGSNAT):c.1776C>T (p.Tyr592=)Mucopolysaccharidosis, MPS-III-C [RCV002604913]likely benign84319943743199437Human1name
156125043CV1992896single nucleotide variantNM_152419.3(HGSNAT):c.1752C>A (p.Val584=)Mucopolysaccharidosis, MPS-III-C [RCV002623093]uncertain significance84319941343199413Human1name
156254137CV2003616single nucleotide variantNM_152419.3(HGSNAT):c.1566G>A (p.Thr522=)Mucopolysaccharidosis, MPS-III-C [RCV002627549]likely benign84319769543197695Human1name
155936108CV2045799single nucleotide variantNM_152419.3(HGSNAT):c.218C>T (p.Ser73Phe)Mucopolysaccharidosis, MPS-III-C [RCV002751469]uncertain significance84314704743147047Human1name
156239968CV2047398single nucleotide variantNM_152419.3(HGSNAT):c.1228C>T (p.Leu410=)Mucopolysaccharidosis, MPS-III-C [RCV002805640]|Retinal dystrophy [RCV003889161]likely benign|uncertain significance84319157343191573Human3name
156340725CV2055366single nucleotide variantNM_152419.3(HGSNAT):c.1533T>C (p.Cys511=)Mucopolysaccharidosis, MPS-III-C [RCV002811185]likely benign84319701643197016Human1name
155999286CV2057324single nucleotide variantNM_152419.3(HGSNAT):c.1110G>C (p.Val370=)Mucopolysaccharidosis, MPS-III-C [RCV002819569]likely benign84318224243182242Human1name
156284339CV2061576single nucleotide variantNM_152419.3(HGSNAT):c.244C>T (p.Gln82Ter)Mucopolysaccharidosis, MPS-III-C [RCV002832951]pathogenic84315858443158584Human1name
156296162CV2065328single nucleotide variantNM_152419.3(HGSNAT):c.1158C>T (p.Ile386=)Mucopolysaccharidosis, MPS-III-C [RCV002856951]likely benign84319150343191503Human1name
156222178CV2067946single nucleotide variantNM_152419.3(HGSNAT):c.1401C>G (p.Ala467=)Mucopolysaccharidosis, MPS-III-C [RCV002829727]likely benign84319378043193780Human1name
155981382CV2070133single nucleotide variantNM_152419.3(HGSNAT):c.1722T>C (p.Tyr574=)Mucopolysaccharidosis, MPS-III-C [RCV002842535]likely benign84319794843197948Human1name
156178824CV2072186single nucleotide variantNM_152419.3(HGSNAT):c.1054T>C (p.Leu352=)Mucopolysaccharidosis, MPS-III-C [RCV002851772]likely benign84318218643182186Human1name
156107748CV2072380deletionNM_152419.3(HGSNAT):c.959del (p.Leu320fs)Mucopolysaccharidosis, MPS-III-C [RCV002870776]pathogenic84317818143178181Human1name
155943635CV2072399single nucleotide variantNM_152419.3(HGSNAT):c.1185C>T (p.Leu395=)Mucopolysaccharidosis, MPS-III-C [RCV002861937]likely benign84319153043191530Human1name
156331727CV2075792single nucleotide variantNM_152419.3(HGSNAT):c.1452T>C (p.Phe484=)Mucopolysaccharidosis, MPS-III-C [RCV002835336]likely benign84319383143193831Human1name
155958182CV2087134single nucleotide variantNM_152419.3(HGSNAT):c.1453T>C (p.Leu485=)Mucopolysaccharidosis, MPS-III-C [RCV002862722]likely benign84319383243193832Human1name
155958503CV2087158single nucleotide variantNM_152419.3(HGSNAT):c.1818G>A (p.Lys606=)Mucopolysaccharidosis, MPS-III-C [RCV002862739]likely benign84319947943199479Human1name
156313986CV2089512single nucleotide variantNM_152419.3(HGSNAT):c.1566G>C (p.Thr522=)Mucopolysaccharidosis, MPS-III-C [RCV002898879]likely benign84319769543197695Human1name
156167056CV2102249single nucleotide variantNM_152419.3(HGSNAT):c.1795C>T (p.Leu599=)Mucopolysaccharidosis, MPS-III-C [RCV002891206]likely benign84319945643199456Human1name
156327501CV2116155single nucleotide variantNM_152419.3(HGSNAT):c.1431C>T (p.Ile477=)Mucopolysaccharidosis, MPS-III-C [RCV002938172]likely benign84319381043193810Human1name
156036659CV2143239deletionNM_152419.3(HGSNAT):c.932del (p.Leu311fs)Mucopolysaccharidosis, MPS-III-C [RCV002999357]pathogenic84317815443178154Human1name
155907877CV2144549single nucleotide variantNM_152419.3(HGSNAT):c.1089G>A (p.Glu363=)Mucopolysaccharidosis, MPS-III-C [RCV003012039]likely benign84318222143182221Human1name
156109828CV2145935single nucleotide variantNM_152419.3(HGSNAT):c.1548C>T (p.Leu516=)Mucopolysaccharidosis, MPS-III-C [RCV003021362]likely benign84319767743197677Human1name
156253056CV2162777single nucleotide variantNM_152419.3(HGSNAT):c.1248T>C (p.Pro416=)Mucopolysaccharidosis, MPS-III-C [RCV003026408]likely benign84319159343191593Human1name
156229007CV2164894single nucleotide variantNM_152419.3(HGSNAT):c.1782C>G (p.Pro594=)Mucopolysaccharidosis, MPS-III-C [RCV003043012]likely benign84319944343199443Human1name
156356589CV2165989single nucleotide variantNM_152419.3(HGSNAT):c.1641T>C (p.Ser547=)Mucopolysaccharidosis, MPS-III-C [RCV003031276]likely benign84319786743197867Human1name
156262114CV2191085single nucleotide variantNM_152419.3(HGSNAT):c.135A>T (p.Arg45Ser)Mucopolysaccharidosis, MPS-III-C [RCV003044154]|Retinal dystrophy [RCV003889211]uncertain significance84314696443146964Human3name
405024387CV3082025single nucleotide variantNM_152419.3(HGSNAT):c.1890G>A (p.Lys630=)Mucopolysaccharidosis, MPS-III-C [RCV003785631]likely benign84319955143199551Human1name
405014721CV3083891single nucleotide variantNM_152419.3(HGSNAT):c.1182G>A (p.Leu394=)Mucopolysaccharidosis, MPS-III-C [RCV003784684]likely benign84319152743191527Human1name
405014780CV3083897single nucleotide variantNM_152419.3(HGSNAT):c.1005T>A (p.Leu335=)Mucopolysaccharidosis, MPS-III-C [RCV003784690]likely benign84317822743178227Human1name
404997340CV3088599single nucleotide variantNM_152419.3(HGSNAT):c.1794G>A (p.Lys598=)Mucopolysaccharidosis, MPS-III-C [RCV003793377]likely benign84319945543199455Human1name
402503349CV3090070single nucleotide variantNM_152419.3(HGSNAT):c.1051C>A (p.Arg351=)Mucopolysaccharidosis, MPS-III-C [RCV003788836]likely benign84318218343182183Human1name
402506156CV3090364single nucleotide variantNM_152419.3(HGSNAT):c.1545G>T (p.Gly515=)Mucopolysaccharidosis, MPS-III-C [RCV003789133]likely benign84319767443197674Human1name
402493640CV3092194duplicationNM_152419.3(HGSNAT):c.523dup (p.Ala175fs)Mucopolysaccharidosis, MPS-III-C [RCV003787813]pathogenic84316146643161467Human1name
405034668CV3093083single nucleotide variantNM_152419.3(HGSNAT):c.1380A>T (p.Val460=)Mucopolysaccharidosis, MPS-III-C [RCV003786434]likely benign84319375943193759Human1name
405035292CV3093136single nucleotide variantNM_152419.3(HGSNAT):c.1878C>A (p.Leu626=)Mucopolysaccharidosis, MPS-III-C [RCV003786487]likely benign84319953943199539Human1name
404992059CV3094320single nucleotide variantNM_152419.3(HGSNAT):c.1485T>C (p.Tyr495=)Mucopolysaccharidosis, MPS-III-C [RCV003782570]likely benign84319696843196968Human1name
405017987CV3094348single nucleotide variantNM_152419.3(HGSNAT):c.1353C>T (p.His451=)Mucopolysaccharidosis, MPS-III-C [RCV003785038]likely benign84319240643192406Human1name
405028201CV3094859single nucleotide variantNM_152419.3(HGSNAT):c.1404T>C (p.Tyr468=)Mucopolysaccharidosis, MPS-III-C [RCV003796221]likely benign84319378343193783Human1name
405055877CV3095116single nucleotide variantNM_152419.3(HGSNAT):c.1510C>T (p.Leu504=)Mucopolysaccharidosis, MPS-III-C [RCV003798430]likely benign84319699343196993Human1name
405011078CV3096664single nucleotide variantNM_152419.3(HGSNAT):c.1800G>A (p.Lys600=)Mucopolysaccharidosis, MPS-III-C [RCV003794653]likely benign84319946143199461Human1name
405027800CV3098118deletionNM_152419.3(HGSNAT):c.451del (p.Cys151fs)Mucopolysaccharidosis, MPS-III-C [RCV003806411]pathogenic84315900243159002Human1name
404979451CV3099422single nucleotide variantNM_152419.3(HGSNAT):c.1416C>T (p.Gly472=)Mucopolysaccharidosis, MPS-III-C [RCV003791250]likely benign84319379543193795Human1name
405003441CV3102170single nucleotide variantNM_152419.3(HGSNAT):c.1095C>T (p.Leu365=)Mucopolysaccharidosis, MPS-III-C [RCV003804216]likely benign84318222743182227Human1name
402524749CV3102585duplicationNM_152419.3(HGSNAT):c.698dup (p.Ser234fs)Mucopolysaccharidosis, MPS-III-C [RCV003790679]pathogenic|likely pathogenic84317064843170649Human1name
404977691CV3102741single nucleotide variantNM_152419.3(HGSNAT):c.1455A>G (p.Leu485=)Mucopolysaccharidosis, MPS-III-C [RCV003790835]likely benign84319383443193834Human1name
405061417CV3102865single nucleotide variantNM_152419.3(HGSNAT):c.1746A>G (p.Val582=)Mucopolysaccharidosis, MPS-III-C [RCV003798855]likely benign84319940743199407Human1name
405043919CV3103808single nucleotide variantNM_152419.3(HGSNAT):c.1344A>G (p.Gly448=)Mucopolysaccharidosis, MPS-III-C [RCV003797526]likely benign84319239743192397Human1name
405169154CV3104180single nucleotide variantNM_152419.3(HGSNAT):c.1419C>T (p.Ile473=)Mucopolysaccharidosis, MPS-III-C [RCV003802857]likely benign84319379843193798Human1name
405170338CV3104283single nucleotide variantNM_152419.3(HGSNAT):c.1195C>T (p.Leu399=)Mucopolysaccharidosis, MPS-III-C [RCV003802960]likely benign84319154043191540Human1name
405015406CV3104447single nucleotide variantNM_152419.3(HGSNAT):c.1026G>A (p.Lys342=)Mucopolysaccharidosis, MPS-III-C [RCV003805316]likely benign84318215843182158Human1name
405173104CV3104726single nucleotide variantNM_152419.3(HGSNAT):c.1806C>T (p.Asn602=)Mucopolysaccharidosis, MPS-III-C [RCV003803224]likely benign84319946743199467Human1name
405009396CV3105999single nucleotide variantNM_152419.3(HGSNAT):c.1480T>C (p.Leu494=)Mucopolysaccharidosis, MPS-III-C [RCV003794497]likely benign84319696343196963Human1name
405016841CV3107045single nucleotide variantNM_152419.3(HGSNAT):c.1104A>G (p.Lys368=)Mucopolysaccharidosis, MPS-III-C [RCV003795215]likely benign84318223643182236Human1name
405056172CV3107928single nucleotide variantNM_152419.3(HGSNAT):c.1221A>G (p.Thr407=)Mucopolysaccharidosis, MPS-III-C [RCV003808674]likely benign84319156643191566Human1name
405037453CV3108745duplicationNM_152419.3(HGSNAT):c.505dup (p.Ala169fs)Mucopolysaccharidosis, MPS-III-C [RCV003807203]|Mucopolysaccharidosis, MPS-III-C [RCV004573333]pathogenic|likely pathogenic84316144843161449Human1name
405063818CV3108790single nucleotide variantNM_152419.3(HGSNAT):c.1536T>C (p.Cys512=)Mucopolysaccharidosis, MPS-III-C [RCV003809200]likely benign84319701943197019Human1name
405008848CV3109013single nucleotide variantNM_152419.3(HGSNAT):c.1101T>C (p.Ala367=)Mucopolysaccharidosis, MPS-III-C [RCV003804680]likely benign84318223343182233Human1name
405159996CV3109757single nucleotide variantNM_152419.3(HGSNAT):c.1707A>G (p.Gly569=)Mucopolysaccharidosis, MPS-III-C [RCV003802116]likely benign84319793343197933Human1name
405069949CV3111150single nucleotide variantNM_152419.3(HGSNAT):c.127A>T (p.Lys43Ter)Mucopolysaccharidosis, MPS-III-C [RCV003809654]pathogenic84314695643146956Human1name
405124687CV3111782duplicationNM_152419.3(HGSNAT):c.793dup (p.Trp265fs)Mucopolysaccharidosis, MPS-III-C [RCV003815255]pathogenic84317235743172358Human1name
405082372CV3113509single nucleotide variantNM_152419.3(HGSNAT):c.1692G>A (p.Lys564=)Mucopolysaccharidosis, MPS-III-C [RCV003810526]likely benign84319791843197918Human1name
405107080CV3113751single nucleotide variantNM_152419.3(HGSNAT):c.1626T>C (p.Tyr542=)Mucopolysaccharidosis, MPS-III-C [RCV003812874]likely benign84319785243197852Human1name
405080616CV3114826single nucleotide variantNM_152419.3(HGSNAT):c.1062G>A (p.Val354=)Mucopolysaccharidosis, MPS-III-C [RCV003810389]likely benign84318219443182194Human1name
11605095CV314511single nucleotide variantNM_152419.3(HGSNAT):c.277G>T (p.Ala93Ser)Inborn genetic diseases [RCV004984855]|Mucopolysaccharidosis, MPS-III-C [RCV000316013]|Mucopolysaccharidosis, MPS-III-C [RCV002058735]likely benign|uncertain significance84315861743158617Human2name
11601683CV314515single nucleotide variantNM_152419.3(HGSNAT):c.1128G>A (p.Ser376=)Mucopolysaccharidosis, MPS-III-C [RCV000284148]|Mucopolysaccharidosis, MPS-III-C [RCV001241541]uncertain significance84318226043182260Human1name
11602046CV314517single nucleotide variantNM_152419.3(HGSNAT):c.1272C>T (p.Gly424=)Mucopolysaccharidosis, MPS-III-C [RCV000287664]|Mucopolysaccharidosis, MPS-III-C [RCV000932800]|Retinal dystrophy [RCV003889871]|not provided [RCV003422359]benign|likely benign|uncertain significance84319232543192325Human3name
11608479CV314592single nucleotide variantNM_152419.3(HGSNAT):c.205G>A (p.Val69Ile)Mucopolysaccharidosis, MPS-III-C [RCV000355499]|Mucopolysaccharidosis, MPS-III-C [RCV000887168]|Retinal dystrophy [RCV003889870]|Retinitis pigmentosa 73 [RCV004799207]likely benign|uncertain significance84314703443147034Human4name
11610052CV314596single nucleotide variantNM_152419.3(HGSNAT):c.1080T>G (p.Ala360=)Mucopolysaccharidosis, MPS-III-C [RCV000376064]|Mucopolysaccharidosis, MPS-III-C [RCV002058736]likely benign|uncertain significance84318221243182212Human1name
597693107CV3685750single nucleotide variantNM_152419.3(HGSNAT):c.103G>A (p.Ala35Thr)Inborn genetic diseases [RCV004985808]uncertain significance84314059943140599Human1name
597858801CV3864841single nucleotide variantNM_152419.3(HGSNAT):c.1782C>T (p.Pro594=)Mucopolysaccharidosis, MPS-III-C [RCV005213898]likely benign84319944343199443Human1name
597839020CV3867627single nucleotide variantNM_152419.3(HGSNAT):c.1242G>A (p.Gly414=)Mucopolysaccharidosis, MPS-III-C [RCV005210822]likely benign84319158743191587Human1name
597892057CV3867989single nucleotide variantNM_152419.3(HGSNAT):c.1509C>T (p.Ile503=)Mucopolysaccharidosis, MPS-III-C [RCV005219017]likely benign84319699243196992Human1name
597893421CV3868163single nucleotide variantNM_152419.3(HGSNAT):c.1098T>C (p.Phe366=)Mucopolysaccharidosis, MPS-III-C [RCV005219192]likely benign84318223043182230Human1name
597881478CV3869133single nucleotide variantNM_152419.3(HGSNAT):c.1827G>A (p.Leu609=)Mucopolysaccharidosis, MPS-III-C [RCV005217389]likely benign84319948843199488Human1name
597908355CV3870458single nucleotide variantNM_152419.3(HGSNAT):c.1596A>G (p.Pro532=)Mucopolysaccharidosis, MPS-III-C [RCV005221509]likely benign84319772543197725Human1name
597874261CV3874877single nucleotide variantNM_152419.3(HGSNAT):c.1713A>G (p.Pro571=)Mucopolysaccharidosis, MPS-III-C [RCV005216353]likely benign84319793943197939Human1name
597844454CV3878774single nucleotide variantNM_152419.3(HGSNAT):c.1230G>A (p.Leu410=)Mucopolysaccharidosis, MPS-III-C [RCV005227104]likely benign84319157543191575Human1name
12906409CV415132deletionNM_152419.3(HGSNAT):c.739del (p.Arg247fs)Mucopolysaccharidosis, MPS-III-C [RCV000666153]|Mucopolysaccharidosis, MPS-III-C [RCV000691847]|Sanfilippo syndrome [RCV003155215]|not provided [RCV000489181]pathogenic84317069043170690Human2name
13486363CV444286single nucleotide variantNM_152419.3(HGSNAT):c.259G>A (p.Val87Ile)Mucopolysaccharidosis, MPS-III-C [RCV001829521]|Mucopolysaccharidosis, MPS-III-C [RCV002525229]|Retinal dystrophy [RCV003889920]|not provided [RCV000522887]likely benign|uncertain significance84315859943158599Human3name
13624942CV523918single nucleotide variantNM_152419.3(HGSNAT):c.1347C>T (p.Asp449=)Mucopolysaccharidosis, MPS-III-C [RCV001497537]likely benign84319240043192400Human1name
14703211CV637223single nucleotide variantNM_152419.3(HGSNAT):c.164T>A (p.Leu55Ter)Mucopolysaccharidosis, MPS-III-C [RCV000807281]pathogenic|likely pathogenic84314699343146993Human1name
15182846CV711548single nucleotide variantNM_152419.3(HGSNAT):c.1623G>A (p.Ser541=)Mucopolysaccharidosis, MPS-III-C [RCV000974735]|Mucopolysaccharidosis, MPS-III-C [RCV001275636]likely benign84319784943197849Human1name
15177602CV723112single nucleotide variantNM_152419.3(HGSNAT):c.1023C>T (p.Asp341=)Mucopolysaccharidosis, MPS-III-C [RCV000884864]|Mucopolysaccharidosis, MPS-III-C [RCV001275631]likely benign84318215543182155Human1name
15126597CV751176single nucleotide variantNM_152419.3(HGSNAT):c.1410C>T (p.Pro470=)Mucopolysaccharidosis, MPS-III-C [RCV000919352]|Mucopolysaccharidosis, MPS-III-C [RCV001275634]likely benign|uncertain significance84319378943193789Human1name
15145327CV766834single nucleotide variantNM_152419.3(HGSNAT):c.1314T>C (p.Ala438=)Mucopolysaccharidosis, MPS-III-C [RCV001467202]likely benign84319236743192367Human1name
15127018CV766835single nucleotide variantNM_152419.3(HGSNAT):c.1617C>T (p.Ser539=)Mucopolysaccharidosis, MPS-III-C [RCV001454264]likely benign84319784343197843Human1name
15100940CV766836single nucleotide variantNM_152419.3(HGSNAT):c.1660C>T (p.Leu554=)not provided [RCV000936707]likely benign84319788643197886Humanname
15114303CV783116single nucleotide variantNM_152419.3(HGSNAT):c.1275T>C (p.Ile425=)Mucopolysaccharidosis, MPS-III-C [RCV001503301]likely benign84319232843192328Human1name
15120687CV783117single nucleotide variantNM_152419.3(HGSNAT):c.1392C>T (p.Thr464=)Mucopolysaccharidosis, MPS-III-C [RCV000979334]likely benign84319377143193771Human1name
15119102CV783118single nucleotide variantNM_152419.3(HGSNAT):c.1644T>A (p.Ser548=)Mucopolysaccharidosis, MPS-III-C [RCV001478720]likely benign84319787043197870Human1name
15130575CV783119single nucleotide variantNM_152419.3(HGSNAT):c.1650C>T (p.Ala550=)Mucopolysaccharidosis, MPS-III-C [RCV001500665]likely benign84319787643197876Human1name
26921325CV834781single nucleotide variantNM_152419.3(HGSNAT):c.145C>A (p.Leu49Met)Mucopolysaccharidosis, MPS-III-C [RCV001060884]|Mucopolysaccharidosis, MPS-III-C [RCV001275623]uncertain significance84314697443146974Human1name
26908564CV834782single nucleotide variantNM_152419.3(HGSNAT):c.154G>A (p.Asp52Asn)Mucopolysaccharidosis, MPS-III-C [RCV001038340]uncertain significance84314698343146983Human1name
28872058CV899647single nucleotide variantNM_152419.3(HGSNAT):c.268A>G (p.Ser90Gly)Mucopolysaccharidosis, MPS-III-C [RCV001164227]uncertain significance84315860843158608Human1name
28909536CV899655single nucleotide variantNM_152419.3(HGSNAT):c.1488C>T (p.Tyr496=)Mucopolysaccharidosis, MPS-III-C [RCV001160692]|Mucopolysaccharidosis, MPS-III-C [RCV001407361]likely benign|uncertain significance84319697143196971Human1name
38489443CV946078single nucleotide variantNM_152419.3(HGSNAT):c.235T>C (p.Cys79Arg)Mucopolysaccharidosis, MPS-III-C [RCV001238418]uncertain significance84315857543158575Human1name
38460538CV946079single nucleotide variantNM_152419.3(HGSNAT):c.284A>C (p.Lys95Thr)Mucopolysaccharidosis, MPS-III-C [RCV001229370]|Mucopolysaccharidosis, MPS-III-C [RCV001828831]uncertain significance84315862443158624Human1name
38457025CV955423single nucleotide variantNM_152419.3(HGSNAT):c.232C>G (p.His78Asp)Mucopolysaccharidosis, MPS-III-C [RCV001245960]uncertain significance84314706143147061Human1name
38496769CV955424single nucleotide variantNM_152419.3(HGSNAT):c.284A>G (p.Lys95Arg)Mucopolysaccharidosis, MPS-III-C [RCV001242771]|Mucopolysaccharidosis, MPS-III-C [RCV001829001]uncertain significance84315862443158624Human1name
40889399CV972012single nucleotide variantNM_152419.3(HGSNAT):c.157C>T (p.Gln53Ter)Mucopolysaccharidosis, MPS-III-C [RCV001264381]likely pathogenic84314698643146986Human1name
40888592CV972013single nucleotide variantNM_152419.3(HGSNAT):c.220G>T (p.Glu74Ter)Mucopolysaccharidosis, MPS-III-C [RCV001263599]likely pathogenic84314704943147049Human1name
40888593CV972014single nucleotide variantNM_152419.3(HGSNAT):c.265C>T (p.Gln89Ter)Mucopolysaccharidosis, MPS-III-C [RCV001263600]|Mucopolysaccharidosis, MPS-III-C [RCV003770370]pathogenic|likely pathogenic84315860543158605Human1name
40888594CV972015single nucleotide variantNM_152419.3(HGSNAT):c.283A>T (p.Lys95Ter)Mucopolysaccharidosis, MPS-III-C [RCV001263601]likely pathogenic84315862343158623Human1name
8654630CV16270duplicationNM_152419.3(HGSNAT):c.1345dup (p.Asp449fs)Mucopolysaccharidosis, MPS-III-C [RCV000001290]|Mucopolysaccharidosis, MPS-III-C [RCV001390806]|Retinitis pigmentosa 73 [RCV000662072]pathogenic|conflicting interpretations of pathogenicity|uncertain significance84319239743192398Human2name
8595350CV16271single nucleotide variantNM_152419.3(HGSNAT):c.848C>T (p.Pro283Leu)Mucopolysaccharidosis, MPS-III-C [RCV000001291]|Mucopolysaccharidosis, MPS-III-C [RCV000763184]|Retinal dystrophy [RCV000504894]|Retinitis pigmentosa 73 [RCV005252654]|Sanfilippo syndrome [RCV003330379]|not provided [RCV000512873]pathogenic|likely pathogenic84317374043173740Human5name
8595351CV16272single nucleotide variantNM_152419.3(HGSNAT):c.962T>G (p.Leu321Ter)Mucopolysaccharidosis, MPS-III-C [RCV000001292]pathogenic84317818443178184Human1name
9688368CV176990single nucleotide variantNM_152419.3(HGSNAT):c.710C>A (p.Pro237Gln)Mucopolysaccharidosis, MPS-III-C [RCV000670920]|Mucopolysaccharidosis, MPS-III-C [RCV001243388]|not provided [RCV001815238]|not specified [RCV000153362]benign|likely benign|conflicting interpretations of pathogenicity|uncertain significance84317066143170661Human1name
156448493CV1950774single nucleotide variantNM_152419.3(HGSNAT):c.531C>G (p.Ile177Met)Mucopolysaccharidosis, MPS-III-C [RCV003120055]uncertain significance84316147543161475Human1name
156405362CV1994367single nucleotide variantNM_152419.3(HGSNAT):c.604T>C (p.Ser202Pro)Mucopolysaccharidosis, MPS-III-C [RCV002658288]uncertain significance84316921343169213Human1name
243056610CV2418837single nucleotide variantNM_152419.3(HGSNAT):c.850T>C (p.Trp284Arg)Mucopolysaccharidosis, MPS-III-C [RCV005060993]likely pathogenic|uncertain significance84317374243173742Human1name
401774404CV2691724duplicationNM_152419.3(HGSNAT):c.1455dup (p.Gly486fs)Inborn genetic diseases [RCV003285741]pathogenic84319383343193834Human1name
401889656CV2758360single nucleotide variantNM_152419.3(HGSNAT):c.311G>C (p.Ser104Thr)Inborn genetic diseases [RCV003368540]uncertain significance84315865143158651Human1name
404994291CV3085260single nucleotide variantNM_152419.3(HGSNAT):c.818A>T (p.Asn273Ile)Mucopolysaccharidosis, MPS-III-C [RCV003782791]likely pathogenic84317238443172384Human1name
402512547CV3087401single nucleotide variantNM_152419.3(HGSNAT):c.852G>A (p.Trp284Ter)Mucopolysaccharidosis, MPS-III-C [RCV003789752]pathogenic|likely pathogenic84317807443178074Human1name
405021501CV3088098single nucleotide variantNM_152419.3(HGSNAT):c.900A>G (p.Ile300Met)Mucopolysaccharidosis, MPS-III-C [RCV003795658]uncertain significance84317812243178122Human1name
405053246CV3098010deletionNM_152419.3(HGSNAT):c.74_75del (p.Pro25fs)Mucopolysaccharidosis, MPS-III-C [RCV003808423]pathogenic84314056743140568Human1name
404981646CV3099964single nucleotide variantNM_152419.3(HGSNAT):c.610G>T (p.Glu204Ter)Mucopolysaccharidosis, MPS-III-C [RCV003791631]pathogenic84316921943169219Human1name
405108718CV3112369deletionNM_152419.3(HGSNAT):c.1401del (p.Tyr468fs)Mucopolysaccharidosis, MPS-III-C [RCV003813212]pathogenic84319377943193779Human1name
405104804CV3113062single nucleotide variantNM_152419.3(HGSNAT):c.557T>A (p.Leu186Ter)Mucopolysaccharidosis, MPS-III-C [RCV003812352]pathogenic84316150143161501Human1name
405262818CV3188376single nucleotide variantNM_152419.3(HGSNAT):c.448G>A (p.Ala150Thr)Retinal dystrophy [RCV003889440]uncertain significance84315899943158999Human2name
405262821CV3188378single nucleotide variantNM_152419.3(HGSNAT):c.636G>C (p.Glu212Asp)Retinal dystrophy [RCV003889442]uncertain significance84317058743170587Human2name
405262822CV3188379single nucleotide variantNM_152419.3(HGSNAT):c.652A>G (p.Arg218Gly)Retinal dystrophy [RCV003889443]uncertain significance84317060343170603Human2name
405262956CV3188381single nucleotide variantNM_152419.3(HGSNAT):c.801C>G (p.Phe267Leu)Retinal dystrophy [RCV003889445]uncertain significance84317236743172367Human2name
405262957CV3188382single nucleotide variantNM_152419.3(HGSNAT):c.820G>C (p.Gly274Arg)Retinal dystrophy [RCV003889446]uncertain significance84317238643172386Human2name
405777198CV3270078single nucleotide variantNM_152419.3(HGSNAT):c.693G>T (p.Trp231Cys)Inborn genetic diseases [RCV004396995]uncertain significance84317064443170644Human1name
407521928CV3437250single nucleotide variantNM_152419.3(HGSNAT):c.422A>G (p.Asn141Ser)Inborn genetic diseases [RCV004630558]uncertain significance84315897343158973Human1name
596932376CV3538996single nucleotide variantNM_152419.3(HGSNAT):c.782G>A (p.Gly261Glu)not provided [RCV004793122]uncertain significance84317234843172348Humanname
596924974CV3541754single nucleotide variantNM_152419.3(HGSNAT):c.743G>A (p.Gly248Glu)Mucopolysaccharidosis, MPS-III-C [RCV004795465]uncertain significance84317069443170694Human1name
596947439CV3548994single nucleotide variantNM_152419.3(HGSNAT):c.890T>A (p.Met297Lys)not provided [RCV004811318]uncertain significance84317811243178112Humanname
597622959CV3550894deletionNM_152419.3(HGSNAT):c.1351del (p.His451fs)Mucopolysaccharidosis, MPS-III-C [RCV004819270]pathogenic84319240443192404Human1name
597830501CV3735425single nucleotide variantNM_152419.3(HGSNAT):c.741G>T (p.Arg247Ser)Mucopolysaccharidosis, MPS-III-C [RCV005055343]likely pathogenic84317069243170692Human1name
597835132CV3864415single nucleotide variantNM_152419.3(HGSNAT):c.821G>C (p.Gly274Ala)Mucopolysaccharidosis, MPS-III-C [RCV005210051]uncertain significance84317371343173713Human1name
597867001CV3869009deletionNM_152419.3(HGSNAT):c.1242del (p.Cys415fs)Mucopolysaccharidosis, MPS-III-C [RCV005215130]pathogenic84319158543191585Human1name
597900408CV3876317duplicationNM_152419.3(HGSNAT):c.1021dup (p.Asp341fs)Mucopolysaccharidosis, MPS-III-C [RCV005220207]pathogenic84318215043182151Human1name
597915661CV3879015single nucleotide variantNM_152419.3(HGSNAT):c.446T>C (p.Ile149Thr)Mucopolysaccharidosis, MPS-III-C [RCV005222551]uncertain significance84315899743158997Human1name
598212546CV4009061single nucleotide variantNM_152419.3(HGSNAT):c.517G>A (p.Gly173Ser)Mucopolysaccharidosis, MPS-III-C [RCV005400675]uncertain significance84316146143161461Human1name
617151313CV4021741deletionNM_152419.3(HGSNAT):c.1361del (p.Gln454fs)not provided [RCV005426702]pathogenic84319241443192414Humanname
26888696CV818746single nucleotide variantNM_152419.3(HGSNAT):c.784G>A (p.Gly262Arg)Mucopolysaccharidosis [RCV001030802]pathogenic|not provided84317235043172350Human1name
26913300CV834783single nucleotide variantNM_152419.3(HGSNAT):c.326C>A (p.Ser109Tyr)Mucopolysaccharidosis, MPS-III-C [RCV001054141]|Mucopolysaccharidosis, MPS-III-C [RCV001275625]|not provided [RCV004590064]uncertain significance84315866643158666Human1name
26919288CV834784single nucleotide variantNM_152419.3(HGSNAT):c.371G>A (p.Arg124Lys)Mucopolysaccharidosis, MPS-III-C [RCV001058809]uncertain significance84315871143158711Human1name
26914233CV834785single nucleotide variantNM_152419.3(HGSNAT):c.826A>G (p.Thr276Ala)Inborn genetic diseases [RCV003160436]|Mucopolysaccharidosis, MPS-III-C [RCV001054838]|Mucopolysaccharidosis, MPS-III-C [RCV001827348]uncertain significance84317371843173718Human2name
26916371CV834791duplicationNM_152419.3(HGSNAT):c.1437dup (p.Ile480fs)Mucopolysaccharidosis, MPS-III-C [RCV001041925]pathogenic84319381443193815Human1name
26909985CV856587single nucleotide variantNM_152419.3(HGSNAT):c.791A>G (p.Tyr264Cys)Retinal dystrophy [RCV001074237]uncertain significance84317235743172357Human2name
28872063CV899648single nucleotide variantNM_152419.3(HGSNAT):c.493C>T (p.Pro165Ser)Mucopolysaccharidosis, MPS-III-C [RCV001164228]|Mucopolysaccharidosis, MPS-III-C [RCV001246133]|Retinal dystrophy [RCV004813819]|not provided [RCV004590110]uncertain significance84315904443159044Human3name
28872072CV899650single nucleotide variantNM_152419.3(HGSNAT):c.688A>G (p.Thr230Ala)Mucopolysaccharidosis, MPS-III-C [RCV001164231]|Mucopolysaccharidosis, MPS-III-C [RCV001882526]|not provided [RCV001796376]likely benign|uncertain significance84317063943170639Human1name
28907116CV899651single nucleotide variantNM_152419.3(HGSNAT):c.710C>T (p.Pro237Leu)Inborn genetic diseases [RCV002558408]|Mucopolysaccharidosis, MPS-III-C [RCV001159324]|Mucopolysaccharidosis, MPS-III-C [RCV002483906]uncertain significance84317066143170661Human2name
28907121CV899652single nucleotide variantNM_152419.3(HGSNAT):c.907C>T (p.Arg303Trp)Mucopolysaccharidosis, MPS-III-C [RCV001159327]|Mucopolysaccharidosis, MPS-III-C [RCV002558409]uncertain significance84317812943178129Human1name
34892089CV915033duplicationNM_152419.3(HGSNAT):c.1271dup (p.Ile425fs)Mucopolysaccharidosis, MPS-III-C [RCV001383041]|Mucopolysaccharidosis, MPS-III-C [RCV004570329]|Retinitis pigmentosa 73 [RCV001250773]|Sanfilippo syndrome [RCV001175525]pathogenic|likely pathogenic84319231943192320Human3name
38485304CV934320single nucleotide variantNM_152419.3(HGSNAT):c.444A>C (p.Glu148Asp)Mucopolysaccharidosis, MPS-III-C [RCV001208417]uncertain significance84315899543158995Human1name
38485545CV946080single nucleotide variantNM_152419.3(HGSNAT):c.317A>G (p.Gln106Arg)Mucopolysaccharidosis, MPS-III-C [RCV001236796]|Mucopolysaccharidosis, MPS-III-C [RCV001828884]|not provided [RCV001312174]uncertain significance84315865743158657Human1name
38457726CV946081single nucleotide variantNM_152419.3(HGSNAT):c.533T>G (p.Ile178Ser)Inborn genetic diseases [RCV005348372]|Mucopolysaccharidosis, MPS-III-C [RCV001228708]|Mucopolysaccharidosis, MPS-III-C [RCV001833978]uncertain significance84316147743161477Human2name
38471848CV946082single nucleotide variantNM_152419.3(HGSNAT):c.679C>T (p.Gln227Ter)Mucopolysaccharidosis, MPS-III-C [RCV001231322]pathogenic84317063043170630Human1name
38498539CV946083single nucleotide variantNM_152419.3(HGSNAT):c.852G>T (p.Trp284Cys)Mucopolysaccharidosis, MPS-III-C [RCV001227815]uncertain significance84317807443178074Human1name
38471363CV946084single nucleotide variantNM_152419.3(HGSNAT):c.940A>G (p.Ile314Val)Mucopolysaccharidosis, MPS-III-C [RCV001231200]uncertain significance84317816243178162Human1name
38494839CV955425single nucleotide variantNM_152419.3(HGSNAT):c.452G>C (p.Cys151Ser)Mucopolysaccharidosis, MPS-III-C [RCV001241568]uncertain significance84315900343159003Human1name
38499539CV955426single nucleotide variantNM_152419.3(HGSNAT):c.619C>T (p.Arg207Cys)Mucopolysaccharidosis, MPS-III-C [RCV001244770]|Mucopolysaccharidosis, MPS-III-C [RCV001835212]uncertain significance84316922843169228Human1name
38457457CV955427single nucleotide variantNM_152419.3(HGSNAT):c.715C>T (p.Arg239Cys)Mucopolysaccharidosis, MPS-III-C [RCV001247922]|Mucopolysaccharidosis, MPS-III-C [RCV001835315]|Retinitis pigmentosa 73 [RCV001250769]|not provided [RCV002265017]pathogenic|likely pathogenic|uncertain significance84317066643170666Human2name
38457568CV962889single nucleotide variantNM_152419.3(HGSNAT):c.743G>C (p.Gly248Ala)Mucopolysaccharidosis, MPS-III-C [RCV001879808]|Retinitis pigmentosa 73 [RCV001250770]likely pathogenic|uncertain significance84317069443170694Human2name
38457580CV962892deletionNM_152419.3(HGSNAT):c.1708del (p.Thr570fs)Retinitis pigmentosa 73 [RCV001250776]pathogenic|likely pathogenic84319793343197933Human1name
38596858CV963657single nucleotide variantNM_152419.3(HGSNAT):c.328A>G (p.Ile110Val)Intellectual disability [RCV001252518]|Mucopolysaccharidosis, MPS-III-C [RCV001879857]likely benign|uncertain significance84315866843158668Human3name
40888595CV972016single nucleotide variantNM_152419.3(HGSNAT):c.391G>T (p.Glu131Ter)Mucopolysaccharidosis, MPS-III-C [RCV001263602]|Mucopolysaccharidosis, MPS-III-C [RCV003770371]pathogenic|likely pathogenic84315894243158942Human1name
40888596CV972017single nucleotide variantNM_152419.3(HGSNAT):c.433G>T (p.Gly145Ter)Mucopolysaccharidosis, MPS-III-C [RCV001263603]likely pathogenic84315898443158984Human1name
40888597CV972018single nucleotide variantNM_152419.3(HGSNAT):c.469G>T (p.Glu157Ter)Mucopolysaccharidosis, MPS-III-C [RCV001263604]likely pathogenic84315902043159020Human1name
40888598CV972019single nucleotide variantNM_152419.3(HGSNAT):c.784G>T (p.Gly262Ter)Mucopolysaccharidosis, MPS-III-C [RCV001263605]likely pathogenic84317235043172350Human1name
40888599CV972020single nucleotide variantNM_152419.3(HGSNAT):c.925A>T (p.Arg309Ter)Mucopolysaccharidosis, MPS-III-C [RCV001263606]|Mucopolysaccharidosis, MPS-III-C [RCV001880063]|Synovial plica syndrome [RCV002267635]pathogenic|likely pathogenic84317814743178147Human2name