ClinVar Miner

List of variants in gene SNTA1 studied for Congenital long QT syndrome

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Total variants: 21
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HGVS dbSNP gnomAD frequency
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.*342C>T rs150740903 0.00900
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.497-7C>T rs116972153 0.00063
NM_003098.3(SNTA1):c.787G>T (p.Ala263Ser) rs150576530 0.00054
NM_003098.3(SNTA1):c.*79C>A rs78892511 0.00040
NM_003098.3(SNTA1):c.1118G>A (p.Arg373His) rs754648214 0.00002
NM_003098.3(SNTA1):c.1205G>A (p.Arg402Gln) rs771369802 0.00002
NM_003098.3(SNTA1):c.1479C>T (p.Phe493=) rs559827815 0.00002
NM_003098.3(SNTA1):c.*6G>A rs565582070 0.00001
NM_003098.3(SNTA1):c.1181G>A (p.Arg394His) rs750278583 0.00001
NM_003098.3(SNTA1):c.1256G>A (p.Arg419His) rs751302839 0.00001
NM_003098.3(SNTA1):c.514G>A (p.Val172Ile) rs775580363 0.00001
NM_003098.3(SNTA1):c.*122G>A rs116151218
NM_003098.3(SNTA1):c.1238-13G>C rs748801869
NM_003098.3(SNTA1):c.651G>A (p.Leu217=) rs886056626

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