List of variants in gene ERCC4 reported as likely benign for not provided

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: 31

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HGVS	dbSNP	gnomAD frequency
NC_000016.10:g.13919990C>G	rs3136040	0.01331
NM_005236.3(ERCC4):c.2624A>G (p.Glu875Gly)	rs1800124	0.01216
NM_005236.3(ERCC4):c.1904+190G>A	rs3136165	0.01167
NM_005236.3(ERCC4):c.389-206C>T	rs112309788	0.01057
NM_005236.3(ERCC4):c.793-69G>T	rs10048099	0.01053
NM_005236.3(ERCC4):c.252C>T (p.Leu84=)	rs3136056	0.00941
NM_005236.3(ERCC4):c.2617A>G (p.Ile873Val)	rs2020957	0.00625
NM_005236.3(ERCC4):c.1213+214G>A	rs74009237	0.00605
NM_005236.3(ERCC4):c.1905-140A>T	rs112050686	0.00509
NM_005236.3(ERCC4):c.1135C>T (p.Pro379Ser)	rs1799802	0.00471
NM_005236.3(ERCC4):c.1446A>G (p.Glu482=)	rs114077770	0.00403
NM_005236.3(ERCC4):c.2724C>T (p.Val908=)	rs3136225	0.00290
NM_005236.3(ERCC4):c.325G>A (p.Ala109Thr)	rs148791570	0.00107
NM_005236.3(ERCC4):c.1563C>G (p.Ser521Arg)	rs41552412	0.00099
NM_005236.3(ERCC4):c.974-6T>C	rs201181735	0.00091
NM_005236.3(ERCC4):c.738G>A (p.Ser246=)	rs146650135	0.00021
NM_005236.3(ERCC4):c.2517C>T (p.Pro839=)	rs200715555	0.00014
NM_005236.3(ERCC4):c.2647G>A (p.Glu883Lys)	rs201652412	0.00012
NM_005236.3(ERCC4):c.1860C>G (p.Leu620=)	rs758451676	0.00009
NM_005236.3(ERCC4):c.1983A>G (p.Ala661=)	rs373237850	0.00009
NM_005236.3(ERCC4):c.1284G>A (p.Ala428=)	rs3136151	0.00007
NM_005236.3(ERCC4):c.2118T>C (p.Ile706=)	rs777766206	0.00002
NM_005236.3(ERCC4):c.2604C>T (p.His868=)	rs370809250	0.00002
NM_005236.3(ERCC4):c.1449A>G (p.Arg483=)	rs1177780470	0.00001
NM_005236.3(ERCC4):c.1632C>T (p.Phe544=)	rs1002156756	0.00001
NM_005236.3(ERCC4):c.1811+10A>G	rs1477624759	0.00001
NM_005236.3(ERCC4):c.2434T>C (p.Leu812=)	rs1295720869	0.00001
NM_005236.3(ERCC4):c.241G>T (p.Val81Phe)	rs55761944
NM_005236.3(ERCC4):c.2424A>G (p.Ala808=)	rs1269027695
NM_005236.3(ERCC4):c.850T>C (p.Leu284=)
NM_005236.3(ERCC4):c.974-72A>G	rs3136121

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