ClinVar Miner

List of variants in gene ERCC4 reported as not provided

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Total variants: 31
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HGVS dbSNP
NM_005236.2(ERCC4):c.1135C>T (p.Pro379Ser) rs1799802
NM_005236.2(ERCC4):c.1244G>A (p.Arg415Gln) rs1800067
NM_005236.2(ERCC4):c.1415C>T (p.Pro472Leu) rs572439259
NM_005236.2(ERCC4):c.1447A>G (p.Arg483Gly) rs587778286
NM_005236.2(ERCC4):c.1488A>T (p.Gln496His) rs146601373
NM_005236.2(ERCC4):c.1523G>A (p.Gly508Glu) rs587778288
NM_005236.2(ERCC4):c.1563C>G (p.Ser521Arg) rs41552412
NM_005236.2(ERCC4):c.1606G>C (p.Val536Leu) rs143347563
NM_005236.2(ERCC4):c.1657A>G (p.Ile553Val) rs376216413
NM_005236.2(ERCC4):c.16C>T (p.Pro6Ser) rs61760160
NM_005236.2(ERCC4):c.1711C>T (p.His571Tyr) rs587778287
NM_005236.2(ERCC4):c.1727G>C (p.Arg576Thr) rs1800068
NM_005236.2(ERCC4):c.176T>A (p.Val59Glu) rs587778283
NM_005236.2(ERCC4):c.1984T>C (p.Ser662Pro) rs2020955
NM_005236.2(ERCC4):c.2017+1G>A rs587777943
NM_005236.2(ERCC4):c.2117T>C (p.Ile706Thr) rs1800069
NM_005236.2(ERCC4):c.211T>C (p.Tyr71His) rs145315496
NM_005236.2(ERCC4):c.217A>G (p.Ile73Val) rs141591400
NM_005236.2(ERCC4):c.2395C>T (p.Arg799Trp) rs121913049
NM_005236.2(ERCC4):c.241G>T (p.Val81Phe) rs55761944
NM_005236.2(ERCC4):c.2477C>T (p.Ala826Val) rs141790888
NM_005236.2(ERCC4):c.2545C>G (p.Gln849Glu) rs374186605
NM_005236.2(ERCC4):c.2579C>A (p.Ala860Asp) rs4986933
NM_005236.2(ERCC4):c.2590C>T (p.Arg864Cys) rs587778284
NM_005236.2(ERCC4):c.2608G>A (p.Val870Ile) rs562305007
NM_005236.2(ERCC4):c.2617A>G (p.Ile873Val) rs2020957
NM_005236.2(ERCC4):c.2624A>G (p.Glu875Gly) rs1800124
NM_005236.2(ERCC4):c.2734G>A (p.Gly912Arg) rs150077735
NM_005236.2(ERCC4):c.79C>T (p.Leu27Phe) rs587778282
NM_005236.2(ERCC4):c.938T>C (p.Leu313Pro) rs150244523
NM_005236.2(ERCC4):c.988G>C (p.Asp330His) rs587778285

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