List of variants in gene WHRN reported as uncertain significance 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: 49

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HGVS	dbSNP	gnomAD frequency
NM_015404.4(WHRN):c.1943C>A (p.Ser648Tyr)	rs142653982	0.00098
NM_015404.4(WHRN):c.2027C>G (p.Pro676Arg)	rs139279977	0.00067
NM_015404.4(WHRN):c.2510G>A (p.Arg837His)	rs55749855	0.00053
NM_015404.4(WHRN):c.1148C>A (p.Thr383Asn)	rs147283064	0.00052
NM_015404.4(WHRN):c.995G>A (p.Arg332Gln)	rs139193948	0.00045
NM_015404.4(WHRN):c.2417C>T (p.Pro806Leu)	rs149897775	0.00036
NM_015404.4(WHRN):c.1381A>C (p.Met461Leu)	rs144878400	0.00022
NM_015404.4(WHRN):c.619G>T (p.Ala207Ser)	rs111033469	0.00021
NM_015404.4(WHRN):c.2354C>T (p.Thr785Ile)	rs201555289	0.00019
NM_015404.4(WHRN):c.2060C>T (p.Pro687Leu)	rs534523640	0.00014
NM_015404.4(WHRN):c.998G>A (p.Ser333Asn)	rs200073414	0.00011
NM_015404.4(WHRN):c.1625G>A (p.Arg542Lys)	rs200040563	0.00010
NM_015404.4(WHRN):c.1222C>A (p.Pro408Thr)	rs368241259	0.00009
NM_015404.4(WHRN):c.1349G>A (p.Arg450His)	rs200377723	0.00007
NM_015404.4(WHRN):c.2540A>G (p.Gln847Arg)	rs545326842	0.00004
NM_015404.4(WHRN):c.958C>T (p.Leu320Phe)	rs780855079	0.00004
NM_015404.4(WHRN):c.2029A>G (p.Ile677Val)	rs758287560	0.00003
NM_015404.4(WHRN):c.35C>T (p.Ser12Leu)	rs760261757	0.00003
NM_015404.4(WHRN):c.44C>T (p.Thr15Ile)	rs727502957	0.00003
NM_015404.4(WHRN):c.1291C>T (p.Arg431Trp)	rs397517256	0.00002
NM_015404.4(WHRN):c.139A>G (p.Thr47Ala)	rs556585167	0.00002
NM_015404.4(WHRN):c.2234G>A (p.Arg745His)	rs555619169	0.00002
NM_015404.4(WHRN):c.2293G>C (p.Gly765Arg)	rs142685292	0.00002
NM_015404.4(WHRN):c.2645G>A (p.Arg882His)	rs760928525	0.00002
NM_015404.4(WHRN):c.1547C>T (p.Thr516Ile)	rs756090687	0.00001
NM_015404.4(WHRN):c.2056C>A (p.Pro686Thr)	rs201690920	0.00001
NM_015404.4(WHRN):c.2284G>A (p.Glu762Lys)	rs757731586	0.00001
NM_015404.4(WHRN):c.2542-1G>A	rs1250528376	0.00001
NM_015404.4(WHRN):c.725G>A (p.Arg242His)	rs727505127	0.00001
NC_000009.11:g.(?_117164359)_(117267737_?)dup
NC_000009.12:g.(?_114402754)_(114504801_?)dup
NM_015404.4(WHRN):c.1126G>T (p.Ala376Ser)	rs545251395
NM_015404.4(WHRN):c.14T>C (p.Leu5Pro)	rs1554747807
NM_015404.4(WHRN):c.1850C>T (p.Ser617Leu)	rs150146590
NM_015404.4(WHRN):c.2364G>T (p.Arg788Ser)	rs1441372523
NM_015404.4(WHRN):c.2418+3G>A	rs876657772
NM_015404.4(WHRN):c.2569C>T (p.Gln857Ter)	rs727504817
NM_015404.4(WHRN):c.2621G>C (p.Gly874Ala)	rs756466784
NM_015404.4(WHRN):c.2644C>A (p.Arg882Ser)	rs150586098
NM_015404.4(WHRN):c.2722T>C (p.Ter908Gln)	rs727505255
NM_015404.4(WHRN):c.321C>G (p.Asp107Glu)	rs766238813
NM_015404.4(WHRN):c.328A>G (p.Thr110Ala)	rs572312301
NM_015404.4(WHRN):c.640C>G (p.Leu214Val)	rs1554735418
NM_015404.4(WHRN):c.676G>C (p.Gly226Arg)	rs727502955
NM_015404.4(WHRN):c.75CGG[2] (p.Gly29del)	rs757435431
NM_015404.4(WHRN):c.914A>G (p.Tyr305Cys)	rs1589199689
NM_015404.4(WHRN):c.919A>G (p.Thr307Ala)	rs2132955317
NM_015404.4(WHRN):c.943G>C (p.Ala315Pro)	rs876657774
NM_015404.4(WHRN):c.955G>T (p.Gly319Trp)	rs143165834

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