List of variants in gene SCN10A reported as benign for Brugada syndrome

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 47

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HGVS	dbSNP	gnomAD frequency
NM_006514.4(SCN10A):c.5137A>G (p.Met1713Val)	rs6599241	1.00000
NM_006514.4(SCN10A):c.4866T>C (p.Ser1622=)	rs6599242	0.93283
NM_006514.4(SCN10A):c.1868-9A>G	rs6599250	0.69912
NM_006514.4(SCN10A):c.884-13T>C	rs7641844	0.30982
NM_006514.4(SCN10A):c.4323A>G (p.Lys1441=)	rs6790627	0.20722
NM_006514.4(SCN10A):c.1476C>T (p.Leu492=)	rs7617919	0.20158
NM_006514.4(SCN10A):c.1284G>A (p.Glu428=)	rs62244070	0.20052
NM_006514.4(SCN10A):c.1525T>C (p.Ser509Pro)	rs7630989	0.08988
NM_006514.4(SCN10A):c.5217C>T (p.Asp1739=)	rs116353929	0.02232
NM_006514.4(SCN10A):c.4710G>A (p.Thr1570=)	rs78425180	0.01966
NM_006514.4(SCN10A):c.4090-19C>T	rs77494117	0.01447
NM_006514.4(SCN10A):c.618A>G (p.Ile206Met)	rs74717885	0.01345
NM_006514.4(SCN10A):c.5089G>A (p.Val1697Ile)	rs77804526	0.00850
NM_006514.4(SCN10A):c.45C>T (p.Arg15=)	rs34314583	0.00684
NM_006514.4(SCN10A):c.4009T>A (p.Ser1337Thr)	rs11711062	0.00451
NM_006514.4(SCN10A):c.4657+16C>T	rs115824540	0.00446
NM_006514.4(SCN10A):c.4656G>A (p.Ala1552=)	rs151182542	0.00431
NM_006514.4(SCN10A):c.1768G>A (p.Gly590Arg)	rs35332705	0.00371
NM_006514.4(SCN10A):c.5657C>T (p.Ala1886Val)	rs142653846	0.00318
NM_006514.4(SCN10A):c.4416C>T (p.Ile1472=)	rs144944369	0.00267
NM_006514.4(SCN10A):c.950+17T>C	rs188914048	0.00231
NM_006514.4(SCN10A):c.1453C>T (p.Arg485Cys)	rs151153639	0.00217
NM_006514.4(SCN10A):c.268C>T (p.Arg90Trp)	rs144270136	0.00148
NM_006514.4(SCN10A):c.5496T>C (p.Thr1832=)	rs112374164	0.00127
NM_006514.4(SCN10A):c.5295G>A (p.Ser1765=)	rs145313578	0.00097
NM_006514.4(SCN10A):c.1867+13C>T	rs138063699	0.00072
NM_006514.4(SCN10A):c.648A>C (p.Thr216=)	rs150977149	0.00060
NM_006514.4(SCN10A):c.4872C>T (p.Phe1624=)	rs149642957	0.00049
NM_006514.4(SCN10A):c.4984G>A (p.Gly1662Ser)	rs151090729	0.00047
NM_006514.4(SCN10A):c.3542C>T (p.Thr1181Met)	rs150773437	0.00026
NM_006514.4(SCN10A):c.5047C>T (p.Pro1683Ser)	rs146999807	0.00025
NM_006514.4(SCN10A):c.2043C>T (p.Phe681=)	rs367743519	0.00024
NM_006514.4(SCN10A):c.4089+12A>T	rs151164057	0.00019
NM_006514.4(SCN10A):c.53C>T (p.Pro18Leu)	rs190176472	0.00019
NM_006514.4(SCN10A):c.1157T>G (p.Phe386Cys)	rs78555408	0.00012
NM_006514.4(SCN10A):c.390-9G>A	rs370917734	0.00009
NM_006514.4(SCN10A):c.5628C>G (p.Thr1876=)	rs147660344	0.00009
NM_006514.4(SCN10A):c.1949T>A (p.Met650Lys)	rs201698323	0.00007
NM_006514.4(SCN10A):c.4515G>A (p.Thr1505=)	rs191624001	0.00006
NM_006514.4(SCN10A):c.462G>A (p.Glu154=)	rs541804553	0.00002
NM_006514.4(SCN10A):c.5834A>G (p.Glu1945Gly)	rs372702302	0.00002
NM_006514.4(SCN10A):c.4379G>A (p.Arg1460Gln)	rs369399424	0.00001
NM_006514.4(SCN10A):c.4680T>G (p.Leu1560=)	rs529845623	0.00001
NM_006514.4(SCN10A):c.1291-4G>A	rs376077984
NM_006514.4(SCN10A):c.1291-5C>T	rs563934615
NM_006514.4(SCN10A):c.285G>T (p.Leu95=)	rs560088419
NM_006514.4(SCN10A):c.4694G>A (p.Ser1565Asn)	rs200063383

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