ClinVar Miner

List of variants in gene ATP7A reported as likely benign for not provided

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Total variants: 34
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HGVS dbSNP
NM_000052.7(ATP7A):c.1009G>A (p.Ala337Thr) rs138039591
NM_000052.7(ATP7A):c.1152T>C (p.Asp384=) rs147225045
NM_000052.7(ATP7A):c.120+194A>G rs139196328
NM_000052.7(ATP7A):c.1251G>T (p.Gly417=) rs781846400
NM_000052.7(ATP7A):c.1273C>T (p.Leu425=) rs781950759
NM_000052.7(ATP7A):c.1302A>C (p.Ala434=) rs782148279
NM_000052.7(ATP7A):c.1543+9C>G rs367977602
NM_000052.7(ATP7A):c.1675G>A (p.Ala559Thr) rs1603383823
NM_000052.7(ATP7A):c.1708-5A>C rs782104249
NM_000052.7(ATP7A):c.1722G>A (p.Thr574=) rs207478437
NM_000052.7(ATP7A):c.1934G>A (p.Arg645Gln) rs782729433
NM_000052.7(ATP7A):c.2277C>G (p.Ala759=) rs1473914623
NM_000052.7(ATP7A):c.2391G>A (p.Leu797=) rs1603385697
NM_000052.7(ATP7A):c.2627-7C>T rs1603386991
NM_000052.7(ATP7A):c.2775A>G (p.Thr925=) rs1603387045
NM_000052.7(ATP7A):c.2917-9C>T rs188421674
NM_000052.7(ATP7A):c.318A>G (p.Thr106=) rs781851530
NM_000052.7(ATP7A):c.3294+907C>T rs139339244
NM_000052.7(ATP7A):c.3374A>G (p.Asn1125Ser) rs782764064
NM_000052.7(ATP7A):c.3449T>C (p.Ile1150Thr) rs201225704
NM_000052.7(ATP7A):c.3659-257G>C rs138431566
NM_000052.7(ATP7A):c.3696G>A (p.Val1232=) rs1557238252
NM_000052.7(ATP7A):c.3903T>C (p.Asp1301=) rs782582761
NM_000052.7(ATP7A):c.4029A>C (p.Ala1343=) rs1603391248
NM_000052.7(ATP7A):c.4226+48A>G rs17218310
NM_000052.7(ATP7A):c.4267C>T (p.Arg1423Trp) rs149079962
NM_000052.7(ATP7A):c.4389T>C (p.Ser1463=) rs371939448
NM_000052.7(ATP7A):c.4414C>T (p.Arg1472Cys) rs782062633
NM_000052.7(ATP7A):c.4467G>C (p.Val1489=) rs1603391708
NM_000052.7(ATP7A):c.513C>T (p.Val171=) rs782643553
NM_000052.7(ATP7A):c.610+108G>A rs148390231
NM_000052.7(ATP7A):c.729G>A (p.Lys243=) rs782326318
NM_000052.7(ATP7A):c.84G>A (p.Gln28=) rs1603378828
NM_000052.7(ATP7A):c.880A>T (p.Asn294Tyr) rs150526992

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