List of variants in gene SCN10A reported as benign for not specified

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: 39

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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.4568G>A (p.Cys1523Tyr)	rs142217269	0.00134
NM_006514.4(SCN10A):c.5295G>A (p.Ser1765=)	rs145313578	0.00097
NM_006514.4(SCN10A):c.648A>C (p.Thr216=)	rs150977149	0.00060
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.969T>C (p.Tyr323=)	rs143668889	0.00023
NM_006514.4(SCN10A):c.3753C>A (p.Thr1251=)	rs144350950	0.00021
NM_006514.4(SCN10A):c.390-9G>A	rs370917734	0.00009
NM_006514.4(SCN10A):c.4956G>A (p.Leu1652=)	rs148256707	0.00007
NM_006514.4(SCN10A):c.3705G>A (p.Ala1235=)	rs147376215	0.00006
NM_006514.4(SCN10A):c.4515G>A (p.Thr1505=)	rs191624001	0.00006
NM_006514.4(SCN10A):c.4660C>T (p.Leu1554=)	rs745999522	0.00006
NM_006514.4(SCN10A):c.1110G>T (p.Gly370=)	rs267599808	0.00004
NM_006514.4(SCN10A):c.4680T>G (p.Leu1560=)	rs529845623	0.00001
NM_006514.4(SCN10A):c.1857C>T (p.Ser619=)	rs374060366
NM_006514.4(SCN10A):c.5137= (p.Met1713=)	rs6599241

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