List of variants in gene WHRN reported as likely 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: 45

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HGVS	dbSNP	gnomAD frequency
NM_015404.4(WHRN):c.1166+18G>A	rs149202009	0.00456
NM_015404.4(WHRN):c.1048C>T (p.Arg350Trp)	rs142990800	0.00147
NM_015404.4(WHRN):c.19G>C (p.Gly7Arg)	rs572671060	0.00141
NM_015404.4(WHRN):c.33C>G (p.Ser11Arg)	rs45527543	0.00130
NM_015404.4(WHRN):c.1149C>T (p.Thr383=)	rs149558159	0.00098
NM_015404.4(WHRN):c.1992G>A (p.Pro664=)	rs142568702	0.00084
NM_015404.4(WHRN):c.1135C>T (p.Arg379Trp)	rs56059137	0.00083
NM_015404.4(WHRN):c.2322C>T (p.Ser774=)	rs55966714	0.00062
NM_015404.4(WHRN):c.1455G>A (p.Pro485=)	rs141807746	0.00055
NM_015404.4(WHRN):c.1075G>A (p.Val359Ile)	rs147500559	0.00053
NM_015404.4(WHRN):c.191C>A (p.Ala64Asp)	rs146655362	0.00053
NM_015404.4(WHRN):c.995G>A (p.Arg332Gln)	rs139193948	0.00045
NM_015404.4(WHRN):c.1678G>A (p.Ala560Thr)	rs182072601	0.00039
NM_015404.4(WHRN):c.1887G>A (p.Pro629=)	rs143443833	0.00035
NM_015404.4(WHRN):c.2112G>T (p.Leu704=)	rs535492772	0.00011
NM_015404.4(WHRN):c.1696G>C (p.Val566Leu)	rs189654215	0.00010
NM_015404.4(WHRN):c.2384G>A (p.Arg795Gln)	rs143763650	0.00010
NM_015404.4(WHRN):c.1611C>T (p.Thr537=)	rs201280818	0.00009
NM_015404.4(WHRN):c.1716C>T (p.Thr572=)	rs760471578	0.00007
NM_015404.4(WHRN):c.1677C>T (p.Asn559=)	rs138127153	0.00005
NM_015404.4(WHRN):c.1176C>T (p.Gly392=)	rs200276167	0.00004
NM_015404.4(WHRN):c.1417-8G>A	rs202228471	0.00004
NM_015404.4(WHRN):c.2073C>T (p.Ser691=)	rs768690928	0.00004
NM_015404.4(WHRN):c.2085G>A (p.Glu695=)	rs140043085	0.00004
NM_015404.4(WHRN):c.2193C>T (p.Ser731=)	rs147358257	0.00004
NM_015404.4(WHRN):c.2203G>A (p.Val735Ile)	rs373552185	0.00004
NM_015404.4(WHRN):c.1596C>T (p.His532=)	rs775240892	0.00003
NM_015404.4(WHRN):c.1360G>A (p.Val454Ile)	rs370178817	0.00002
NM_015404.4(WHRN):c.1578T>C (p.Gly526=)	rs111033438	0.00001
NM_015404.4(WHRN):c.1725G>A (p.Gly575=)	rs1333495064	0.00001
NM_015404.4(WHRN):c.1833C>T (p.Ser611=)	rs752505729	0.00001
NM_015404.4(WHRN):c.2484C>T (p.Ile828=)	rs777780045	0.00001
NM_015404.4(WHRN):c.376G>A (p.Ala126Thr)	rs1444564272	0.00001
NM_015404.4(WHRN):c.690C>T (p.Thr230=)	rs779112096	0.00001
NM_015404.4(WHRN):c.1158C>G (p.Asn386Lys)	rs397517253
NM_015404.4(WHRN):c.1251C>T (p.Ser417=)	rs1554719002
NM_015404.4(WHRN):c.1542G>A (p.Gly514=)	rs397517257
NM_015404.4(WHRN):c.1626+9C>A	rs727504908
NM_015404.4(WHRN):c.171G>A (p.Gln57=)	rs578204125
NM_015404.4(WHRN):c.1824G>A (p.Gln608=)	rs755074681
NM_015404.4(WHRN):c.2333G>A (p.Arg778Gln)	rs727505188
NM_015404.4(WHRN):c.2455G>A (p.Val819Met)	rs1589057203
NM_015404.4(WHRN):c.2644C>T (p.Arg882Cys)	rs150586098
NM_015404.4(WHRN):c.427T>C (p.Leu143=)	rs727502956
NM_015404.4(WHRN):c.744G>A (p.Ser248=)	rs397517259

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