List of variants in gene SCN5A reported as benign by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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: 30

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HGVS	dbSNP	gnomAD frequency
NM_000335.5(SCN5A):c.87A>G (p.Ala29=)	rs6599230	0.80621
NM_000335.5(SCN5A):c.5454T>C (p.Asp1818=)	rs1805126	0.44288
NM_000335.5(SCN5A):c.1673A>G (p.His558Arg)	rs1805124	0.24768
NM_000335.5(SCN5A):c.1141-3C>A	rs41312433	0.16821
NM_000335.5(SCN5A):c.5841C>T (p.Ile1947=)	rs13324293	0.06728
NM_000335.5(SCN5A):c.4845C>T (p.Phe1615=)	rs41315495	0.05498
NM_000335.5(SCN5A):c.100C>T (p.Arg34Cys)	rs6791924	0.03086
NM_000335.5(SCN5A):c.1302C>T (p.Phe434=)	rs41313699	0.01360
NM_000335.5(SCN5A):c.1571C>A (p.Ser524Tyr)	rs41313691	0.01184
NM_000335.5(SCN5A):c.4215G>A (p.Gly1405=)	rs41311123	0.00859
NM_000335.5(SCN5A):c.1587T>C (p.Ile529=)	rs45624133	0.00575
NM_000335.5(SCN5A):c.1743G>A (p.Ser581=)	rs41313687	0.00537
NM_000335.5(SCN5A):c.3508+10C>T	rs41258454	0.00510
NM_000335.5(SCN5A):c.717C>T (p.Ile239=)	rs41285129	0.00407
NM_000335.5(SCN5A):c.4434+13C>T	rs148598985	0.00361
NM_000335.5(SCN5A):c.1017C>T (p.Tyr339=)	rs17215493	0.00354
NM_000335.5(SCN5A):c.1381T>G (p.Leu461Val)	rs41313697	0.00352
NM_000335.5(SCN5A):c.1569T>A (p.Arg523=)	rs41313693	0.00351
NM_000335.5(SCN5A):c.4506C>T (p.Ser1502=)	rs45548237	0.00350
NM_000335.5(SCN5A):c.1068T>C (p.Asp356=)	rs41313703	0.00349
NM_000335.5(SCN5A):c.2436+12G>A	rs41312419	0.00284
NM_000335.5(SCN5A):c.486C>T (p.Tyr162=)	rs45489099	0.00267
NM_000335.5(SCN5A):c.1890+14G>A	rs145427253	0.00252
NM_000335.5(SCN5A):c.3575G>A (p.Arg1192Gln)	rs41261344	0.00222
NM_000335.5(SCN5A):c.354C>T (p.His118=)	rs45533640	0.00207
NM_000335.5(SCN5A):c.1681C>T (p.Leu561=)	rs45522138	0.00196
NM_000335.5(SCN5A):c.1236C>T (p.Val412=)	rs45565936	0.00114
NM_000335.5(SCN5A):c.5357G>A (p.Ser1786Asn)	rs199473316	0.00063
NM_000335.5(SCN5A):c.3618C>T (p.Phe1206=)	rs184934308	0.00009
NM_000335.5(SCN5A):c.5848G>T (p.Val1950Leu)	rs41315493

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