ClinVar Miner

List of variants in gene SNTA1 studied for Long QT syndrome 12

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Total variants: 89
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HGVS dbSNP gnomAD frequency
NM_003098.3(SNTA1):c.909+30T>C rs291694 0.69088
NM_003098.3(SNTA1):c.807T>C (p.Asn269=) rs73270015 0.02196
NM_003098.3(SNTA1):c.*343G>A rs41305789 0.02092
NM_003098.3(SNTA1):c.1350C>T (p.Phe450=) rs116747979 0.01203
NM_003098.3(SNTA1):c.828G>A (p.Lys276=) rs35938843 0.00969
NM_003098.3(SNTA1):c.555C>T (p.Val185=) rs34995247 0.00948
NM_003098.3(SNTA1):c.317G>A (p.Arg106Gln) rs75025585 0.00904
NM_003098.3(SNTA1):c.*342C>T rs150740903 0.00900
NM_003098.3(SNTA1):c.166C>T (p.Pro56Ser) rs573772189 0.00585
NM_003098.3(SNTA1):c.701+10G>A rs6057846 0.00419
NM_003098.3(SNTA1):c.1426-5T>C rs183939417 0.00221
NM_003098.3(SNTA1):c.770C>G (p.Ala257Gly) rs56157422 0.00217
NM_003098.3(SNTA1):c.221C>T (p.Pro74Leu) rs572545726 0.00198
NM_003098.3(SNTA1):c.993C>T (p.Arg331=) rs143309917 0.00125
NM_003098.3(SNTA1):c.984C>T (p.Pro328=) rs138863915 0.00121
NM_003098.3(SNTA1):c.1488C>A (p.Ala496=) rs34901081 0.00106
NM_003098.3(SNTA1):c.440C>A (p.Thr147Asn) rs141724500 0.00067
NM_003098.3(SNTA1):c.497-7C>T rs116972153 0.00063
NM_003098.3(SNTA1):c.787G>T (p.Ala263Ser) rs150576530 0.00054
NM_003098.3(SNTA1):c.619C>T (p.Arg207Trp) rs139537086 0.00044
NM_003098.3(SNTA1):c.784A>C (p.Thr262Pro) rs200316080 0.00041
NM_003098.3(SNTA1):c.*79C>A rs78892511 0.00040
NM_003098.3(SNTA1):c.210G>C (p.Pro70=) rs751651742 0.00039
NM_003098.3(SNTA1):c.909+17G>T rs376695170 0.00021
NM_003098.3(SNTA1):c.566C>T (p.Ser189Leu) rs144860423 0.00020
NM_003098.3(SNTA1):c.*231C>T rs187657721 0.00018
NM_003098.3(SNTA1):c.1088A>C (p.Glu363Ala) rs147964932 0.00017
NM_003098.3(SNTA1):c.1442C>T (p.Ser481Leu) rs370531842 0.00007
NM_003098.3(SNTA1):c.*132C>T rs757013849 0.00006
NM_003098.3(SNTA1):c.1147G>A (p.Val383Met) rs767361112 0.00006
NM_003098.3(SNTA1):c.1238-14T>C rs369876616 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.1340G>A (p.Arg447Gln) rs752729935 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.1309G>A (p.Glu437Lys) rs371648806 0.00003
NM_003098.3(SNTA1):c.160G>C (p.Gly54Arg) rs786205848 0.00003
NM_003098.3(SNTA1):c.817C>T (p.Pro273Ser) rs750459988 0.00003
NM_003098.3(SNTA1):c.1106G>A (p.Arg369His) rs1012069434 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.1479C>T (p.Phe493=) rs559827815 0.00002
NM_003098.3(SNTA1):c.538A>G (p.Thr180Ala) rs747367304 0.00002
NM_003098.3(SNTA1):c.620G>A (p.Arg207Gln) rs771180054 0.00002
NM_003098.3(SNTA1):c.668C>T (p.Ser223Leu) rs779370807 0.00002
NM_003098.3(SNTA1):c.*333G>A rs1222182431 0.00001
NM_003098.3(SNTA1):c.*6G>A rs565582070 0.00001
NM_003098.3(SNTA1):c.1021G>A (p.Ala341Thr) rs754242619 0.00001
NM_003098.3(SNTA1):c.1169C>T (p.Ala390Val) rs121434500 0.00001
NM_003098.3(SNTA1):c.1181G>A (p.Arg394His) rs750278583 0.00001
NM_003098.3(SNTA1):c.1255C>T (p.Arg419Cys) rs375515058 0.00001
NM_003098.3(SNTA1):c.1256G>A (p.Arg419His) rs751302839 0.00001
NM_003098.3(SNTA1):c.1339C>T (p.Arg447Ter) rs1187536758 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.1486G>C (p.Ala496Pro) rs1463586615 0.00001
NM_003098.3(SNTA1):c.1504G>A (p.Gly502Arg) rs768377696 0.00001
NM_003098.3(SNTA1):c.316C>T (p.Arg106Trp) rs552509775 0.00001
NM_003098.3(SNTA1):c.375G>C (p.Gln125His) rs201421292 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.526T>C (p.Phe176Leu) rs781703999 0.00001
NM_003098.3(SNTA1):c.719C>T (p.Ser240Leu) rs35168199 0.00001
NM_003098.3(SNTA1):c.759T>A (p.Asp253Glu) rs759487225 0.00001
NM_003098.3(SNTA1):c.*122G>A rs116151218
NM_003098.3(SNTA1):c.*412G>C rs566401281
NM_003098.3(SNTA1):c.1003_1021dup (p.Ala341fs) rs775891730
NM_003098.3(SNTA1):c.1025C>G (p.Pro342Arg) rs1989758393
NM_003098.3(SNTA1):c.1238-13G>C rs748801869
NM_003098.3(SNTA1):c.1244C>T (p.Thr415Met) rs533902889
NM_003098.3(SNTA1):c.1283A>G (p.Asp428Gly) rs1390997295
NM_003098.3(SNTA1):c.1487C>T (p.Ala496Val)
NM_003098.3(SNTA1):c.1498C>T (p.Arg500Cys) rs786205426
NM_003098.3(SNTA1):c.185C>A (p.Ala62Glu) rs1990630503
NM_003098.3(SNTA1):c.194A>G (p.Asn65Ser) rs1135401951
NM_003098.3(SNTA1):c.312C>A (p.Gly104=) rs533476140
NM_003098.3(SNTA1):c.370G>A (p.Asp124Asn) rs1430826527
NM_003098.3(SNTA1):c.651G>A (p.Leu217=) rs886056626
NM_003098.3(SNTA1):c.669G>A (p.Ser223=) rs199762207
NM_003098.3(SNTA1):c.740T>G (p.Leu247Arg) rs1989777102
NM_003098.3(SNTA1):c.770C>T (p.Ala257Val) rs56157422
NM_003098.3(SNTA1):c.816G>T (p.Thr272=) rs371028127
NM_003098.3(SNTA1):c.910-3C>T rs1989763108

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