ClinVar Miner

List of variants in gene SNTA1 reported as uncertain significance for Cardiovascular phenotype

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Total variants: 86
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HGVS dbSNP gnomAD frequency
NM_003098.3(SNTA1):c.1157C>T (p.Pro386Leu) rs200865199 0.00019
NM_003098.3(SNTA1):c.1105C>T (p.Arg369Cys) rs369968387 0.00007
NM_003098.3(SNTA1):c.1442C>T (p.Ser481Leu) rs370531842 0.00007
NM_003098.3(SNTA1):c.1147G>A (p.Val383Met) rs767361112 0.00006
NM_003098.3(SNTA1):c.1015C>T (p.Arg339Cys) rs138164106 0.00005
NM_003098.3(SNTA1):c.782C>T (p.Ala261Val) rs139467962 0.00005
NM_003098.3(SNTA1):c.1180C>T (p.Arg394Cys) rs567451585 0.00004
NM_003098.3(SNTA1):c.388T>C (p.Phe130Leu) rs199964677 0.00004
NM_003098.3(SNTA1):c.452C>T (p.Ala151Val) rs772936861 0.00004
NM_003098.3(SNTA1):c.556G>A (p.Gly186Ser) rs200755101 0.00004
NM_003098.3(SNTA1):c.992G>A (p.Arg331His) rs575431717 0.00004
NM_003098.3(SNTA1):c.776C>T (p.Ser259Leu) rs774643587 0.00003
NM_003098.3(SNTA1):c.817C>T (p.Pro273Ser) rs750459988 0.00003
NM_003098.3(SNTA1):c.1109C>T (p.Thr370Met) rs746227626 0.00002
NM_003098.3(SNTA1):c.1118G>A (p.Arg373His) rs754648214 0.00002
NM_003098.3(SNTA1):c.1204C>T (p.Arg402Trp) rs373387978 0.00002
NM_003098.3(SNTA1):c.1205G>A (p.Arg402Gln) rs771369802 0.00002
NM_003098.3(SNTA1):c.1388T>G (p.Leu463Arg) rs188835994 0.00002
NM_003098.3(SNTA1):c.668C>T (p.Ser223Leu) rs779370807 0.00002
NM_003098.3(SNTA1):c.1021G>A (p.Ala341Thr) rs754242619 0.00001
NM_003098.3(SNTA1):c.1151A>G (p.Glu384Gly) rs1365956176 0.00001
NM_003098.3(SNTA1):c.1162G>A (p.Glu388Lys) rs570991600 0.00001
NM_003098.3(SNTA1):c.1169C>T (p.Ala390Val) rs121434500 0.00001
NM_003098.3(SNTA1):c.1279A>G (p.Ile427Val) rs151158866 0.00001
NM_003098.3(SNTA1):c.1325G>A (p.Arg442Gln) rs746800138 0.00001
NM_003098.3(SNTA1):c.1394T>C (p.Phe465Ser) rs774908810 0.00001
NM_003098.3(SNTA1):c.1425+1G>A rs113809208 0.00001
NM_003098.3(SNTA1):c.1484C>T (p.Ser495Leu) rs144006909 0.00001
NM_003098.3(SNTA1):c.200C>T (p.Ala67Val) rs536755693 0.00001
NM_003098.3(SNTA1):c.316C>T (p.Arg106Trp) rs552509775 0.00001
NM_003098.3(SNTA1):c.344C>A (p.Ser115Tyr) rs1359697782 0.00001
NM_003098.3(SNTA1):c.364G>A (p.Ala122Thr) rs151113230 0.00001
NM_003098.3(SNTA1):c.403A>C (p.Ile135Leu) rs756587722 0.00001
NM_003098.3(SNTA1):c.419G>C (p.Gly140Ala) rs768194552 0.00001
NM_003098.3(SNTA1):c.497-5A>G rs202178576 0.00001
NM_003098.3(SNTA1):c.514G>A (p.Val172Ile) rs775580363 0.00001
NM_003098.3(SNTA1):c.759T>A (p.Asp253Glu) rs759487225 0.00001
NM_003098.3(SNTA1):c.766A>T (p.Ser256Cys) rs192115867 0.00001
NM_003098.3(SNTA1):c.773G>A (p.Arg258Lys) rs776064801 0.00001
NM_003098.3(SNTA1):c.955A>G (p.Lys319Glu) rs766990229 0.00001
NM_003098.3(SNTA1):c.991C>T (p.Arg331Cys) rs769528459 0.00001
NM_003098.3(SNTA1):c.1015del (p.Arg339fs)
NM_003098.3(SNTA1):c.1018A>G (p.Thr340Ala)
NM_003098.3(SNTA1):c.1061C>A (p.Ser354Tyr) rs1200381592
NM_003098.3(SNTA1):c.1081G>A (p.Asp361Asn)
NM_003098.3(SNTA1):c.1099G>C (p.Ala367Pro)
NM_003098.3(SNTA1):c.1114A>T (p.Thr372Ser)
NM_003098.3(SNTA1):c.1133C>T (p.Thr378Ile)
NM_003098.3(SNTA1):c.1213G>T (p.Glu405Ter)
NM_003098.3(SNTA1):c.1238-1G>T
NM_003098.3(SNTA1):c.1244C>T (p.Thr415Met) rs533902889
NM_003098.3(SNTA1):c.1258C>T (p.Pro420Ser)
NM_003098.3(SNTA1):c.1287G>C (p.Lys429Asn) rs955414123
NM_003098.3(SNTA1):c.1361A>G (p.Gln454Arg)
NM_003098.3(SNTA1):c.1419C>T (p.Gly473=)
NM_003098.3(SNTA1):c.1426-1G>A
NM_003098.3(SNTA1):c.1450A>G (p.Lys484Glu)
NM_003098.3(SNTA1):c.1471C>T (p.His491Tyr)
NM_003098.3(SNTA1):c.1499G>A (p.Arg500His)
NM_003098.3(SNTA1):c.149G>A (p.Gly50Asp)
NM_003098.3(SNTA1):c.157C>G (p.Pro53Ala)
NM_003098.3(SNTA1):c.178G>A (p.Glu60Lys)
NM_003098.3(SNTA1):c.190C>G (p.Leu64Val)
NM_003098.3(SNTA1):c.242T>C (p.Leu81Pro) rs2146814680
NM_003098.3(SNTA1):c.338T>G (p.Leu113Arg)
NM_003098.3(SNTA1):c.340A>T (p.Ile114Phe)
NM_003098.3(SNTA1):c.346A>G (p.Lys116Glu)
NM_003098.3(SNTA1):c.377C>T (p.Thr126Ile)
NM_003098.3(SNTA1):c.386T>C (p.Leu129Pro)
NM_003098.3(SNTA1):c.454G>A (p.Val152Met)
NM_003098.3(SNTA1):c.500A>G (p.Lys167Arg)
NM_003098.3(SNTA1):c.521C>T (p.Pro174Leu)
NM_003098.3(SNTA1):c.590G>T (p.Arg197Leu)
NM_003098.3(SNTA1):c.602C>T (p.Ser201Phe)
NM_003098.3(SNTA1):c.614C>T (p.Thr205Ile)
NM_003098.3(SNTA1):c.702G>T (p.Arg234Ser)
NM_003098.3(SNTA1):c.751G>A (p.Ala251Thr)
NM_003098.3(SNTA1):c.761A>G (p.Glu254Gly)
NM_003098.3(SNTA1):c.770C>T (p.Ala257Val) rs56157422
NM_003098.3(SNTA1):c.793C>T (p.Gln265Ter) rs373610918
NM_003098.3(SNTA1):c.860G>A (p.Ser287Asn) rs780098159
NM_003098.3(SNTA1):c.869G>A (p.Gly290Glu)
NM_003098.3(SNTA1):c.896_899del (p.Gly298_Trp299insTer)
NM_003098.3(SNTA1):c.920G>C (p.Gly307Ala)
NM_003098.3(SNTA1):c.938T>C (p.Leu313Pro)
NM_003098.3(SNTA1):c.985G>A (p.Glu329Lys)

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