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49 records found for search term Mta1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405791390CV3368782single nucleotide variantNM_004689.4(MTA1):c.224C>T (p.Ala75Val)not specified [RCV004506034]uncertain significance14105449392105449392Humanname
407475805CV3447336single nucleotide variantNM_004689.4(MTA1):c.184C>A (p.His62Asn)not specified [RCV004638437]uncertain significance14105445505105445505Humanname
15139143CV739151single nucleotide variantNM_004689.4(MTA1):c.1956C>T (p.Asp652=)not provided [RCV000899099]benign14105469951105469951Humanname
156241516CV2203872single nucleotide variantNM_004689.4(MTA1):c.881A>G (p.Asn294Ser)not specified [RCV004069927]likely benign14105460892105460892Humanname
155979503CV2222873single nucleotide variantNM_004689.4(MTA1):c.710G>A (p.Ser237Asn)not specified [RCV004101695]uncertain significance14105460414105460414Humanname
156091322CV2389443single nucleotide variantNM_004689.4(MTA1):c.553G>A (p.Glu185Lys)not specified [RCV004238169]uncertain significance14105458272105458272Humanname
405791396CV3368784single nucleotide variantNM_004689.4(MTA1):c.414G>C (p.Lys138Asn)not specified [RCV004506036]uncertain significance14105450306105450306Humanname
405791415CV3368790single nucleotide variantNM_004689.4(MTA1):c.611C>G (p.Pro204Arg)not specified [RCV004506042]uncertain significance14105458330105458330Humanname
598214640CV3989830single nucleotide variantNM_004689.4(MTA1):c.579G>T (p.Arg193Ser)not specified [RCV005378608]uncertain significance14105458298105458298Humanname
598180596CV3989831single nucleotide variantNM_004689.4(MTA1):c.407C>T (p.Ser136Leu)not specified [RCV005372144]uncertain significance14105450299105450299Humanname
598180605CV3989833single nucleotide variantNM_004689.4(MTA1):c.727G>A (p.Ala243Thr)not specified [RCV005372146]uncertain significance14105460431105460431Humanname
156066907CV2236941single nucleotide variantNM_004689.4(MTA1):c.1855C>T (p.Arg619Trp)not specified [RCV004112939]uncertain significance14105469850105469850Humanname
156267620CV2244043single nucleotide variantNM_004689.4(MTA1):c.1436C>T (p.Thr479Met)not specified [RCV004108526]uncertain significance14105464765105464765Humanname
155923724CV2248594single nucleotide variantNM_004689.4(MTA1):c.2024C>T (p.Ser675Leu)not specified [RCV004121783]uncertain significance14105470091105470091Humanname
155996739CV2250484single nucleotide variantNM_004689.4(MTA1):c.1138A>C (p.Thr380Pro)not specified [RCV004127350]uncertain significance14105464093105464093Humanname
155959985CV2252660single nucleotide variantNM_004689.4(MTA1):c.1385A>C (p.Lys462Thr)not specified [RCV004118524]uncertain significance14105464714105464714Humanname
155931603CV2293611single nucleotide variantNM_004689.4(MTA1):c.1827C>A (p.His609Gln)not specified [RCV004153127]uncertain significance14105469480105469480Humanname
156016060CV2299055single nucleotide variantNM_004689.4(MTA1):c.1582C>A (p.Gln528Lys)not specified [RCV004158571]uncertain significance14105465141105465141Humanname
156160808CV2319409single nucleotide variantNM_004689.4(MTA1):c.1636C>T (p.Arg546Cys)not specified [RCV004184998]uncertain significance14105466437105466437Humanname
156352821CV2324052single nucleotide variantNM_004689.4(MTA1):c.1642C>G (p.Pro548Ala)not specified [RCV004178350]uncertain significance14105466443105466443Humanname
155915700CV2339187single nucleotide variantNM_004689.4(MTA1):c.1360C>G (p.Pro454Ala)not specified [RCV004187222]uncertain significance14105464689105464689Humanname
156329759CV2342454single nucleotide variantNM_004689.4(MTA1):c.1354G>A (p.Gly452Ser)not specified [RCV004194058]uncertain significance14105464683105464683Humanname
156009273CV2361982single nucleotide variantNM_004689.4(MTA1):c.2122G>C (p.Asp708His)not specified [RCV004207748]uncertain significance14105470189105470189Humanname
156136536CV2364974single nucleotide variantNM_004689.4(MTA1):c.2116G>A (p.Val706Ile)not specified [RCV004222267]uncertain significance14105470183105470183Humanname
156197190CV2367296single nucleotide variantNM_004689.4(MTA1):c.1643C>G (p.Pro548Arg)not specified [RCV004215714]uncertain significance14105466444105466444Humanname
401750293CV2696007single nucleotide variantNM_004689.4(MTA1):c.1609G>C (p.Val537Leu)not specified [RCV004308266]uncertain significance14105465168105465168Humanname
401884716CV2786555single nucleotide variantNM_004689.4(MTA1):c.2045G>A (p.Arg682His)not specified [RCV004363702]uncertain significance14105470112105470112Humanname
405791367CV3368775single nucleotide variantNM_004689.4(MTA1):c.2111C>T (p.Ala704Val)not specified [RCV004506027]uncertain significance14105470178105470178Humanname
405791020CV3372696single nucleotide variantNM_004689.4(MTA1):c.1089T>G (p.Asn363Lys)not specified [RCV004505948]uncertain significance14105464044105464044Humanname
405791081CV3372713single nucleotide variantNM_004689.4(MTA1):c.1385A>G (p.Lys462Arg)not specified [RCV004505965]uncertain significance14105464714105464714Humanname
405791280CV3372749single nucleotide variantNM_004689.4(MTA1):c.1657G>A (p.Val553Met)not specified [RCV004506001]uncertain significance14105466458105466458Humanname
405791304CV3372756single nucleotide variantNM_004689.4(MTA1):c.1696G>A (p.Ala566Thr)not specified [RCV004506008]uncertain significance14105466497105466497Humanname
405791331CV3372764single nucleotide variantNM_004689.4(MTA1):c.1925C>A (p.Pro642Gln)not specified [RCV004506016]uncertain significance14105469920105469920Humanname
407507059CV3447337single nucleotide variantNM_004689.4(MTA1):c.1842C>G (p.His614Gln)not specified [RCV004646667]uncertain significance14105469495105469495Humanname
407507064CV3447339single nucleotide variantNM_004689.4(MTA1):c.1589T>C (p.Val530Ala)not specified [RCV004646669]uncertain significance14105465148105465148Humanname
597638787CV3564258single nucleotide variantNM_004689.4(MTA1):c.1459C>T (p.Arg487Cys)not specified [RCV004824994]uncertain significance14105464788105464788Humanname
597648064CV3564260single nucleotide variantNM_004689.4(MTA1):c.1105G>A (p.Val369Ile)not specified [RCV004833320]uncertain significance14105464060105464060Humanname
597648070CV3564261single nucleotide variantNM_004689.4(MTA1):c.1691C>T (p.Thr564Met)not specified [RCV004833321]uncertain significance14105466492105466492Humanname
597648077CV3564262single nucleotide variantNM_004689.4(MTA1):c.1912G>T (p.Gly638Cys)not specified [RCV004833322]uncertain significance14105469907105469907Humanname
597648084CV3564263single nucleotide variantNM_004689.4(MTA1):c.1721A>G (p.Asn574Ser)not specified [RCV004833323]uncertain significance14105466522105466522Humanname
597638792CV3564264single nucleotide variantNM_004689.4(MTA1):c.1463A>G (p.Glu488Gly)not specified [RCV004824995]uncertain significance14105464792105464792Humanname
597648091CV3564265single nucleotide variantNM_004689.4(MTA1):c.1351C>T (p.His451Tyr)not specified [RCV004833324]uncertain significance14105464680105464680Humanname
597638798CV3564266single nucleotide variantNM_004689.4(MTA1):c.1123G>A (p.Gly375Ser)not specified [RCV004824996]uncertain significance14105464078105464078Humanname
597648096CV3564267single nucleotide variantNM_004689.4(MTA1):c.2081A>C (p.Gln694Pro)not specified [RCV004833325]uncertain significance14105470148105470148Humanname
597648104CV3564268single nucleotide variantNM_004689.4(MTA1):c.2082G>C (p.Gln694His)not specified [RCV004833326]uncertain significance14105470149105470149Humanname
598180589CV3989829single nucleotide variantNM_004689.4(MTA1):c.1568C>T (p.Pro523Leu)not specified [RCV005372143]uncertain significance14105465127105465127Humanname
598180602CV3989832single nucleotide variantNM_004689.4(MTA1):c.1438C>T (p.Arg480Trp)not specified [RCV005372145]uncertain significance14105464767105464767Humanname
15161041CV702791single nucleotide variantNM_004689.4(MTA1):c.1666G>A (p.Val556Met)not provided [RCV000947600]benign14105466467105466467Humanname
21074541CV796982single nucleotide variantNM_004689.4(MTA1):c.1424C>T (p.Thr475Met)not provided [RCV000995268]|not specified [RCV004030190]uncertain significance14105464753105464753Humanname