ClinVar Miner

List of variants in gene ATRX reported as likely benign for not specified

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Gene type:
ClinVar version:
Total variants: 29
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HGVS dbSNP
NM_000489.5(ATRX):c.134-3T>A rs587780287
NM_000489.5(ATRX):c.134-9C>T rs782350220
NM_000489.5(ATRX):c.1438A>G (p.Thr480Ala) rs587780284
NM_000489.5(ATRX):c.1467C>T (p.Thr489=) rs199929884
NM_000489.5(ATRX):c.1633C>G (p.Gln545Glu) rs35738915
NM_000489.5(ATRX):c.1868A>G (p.Lys623Arg) rs145678415
NM_000489.5(ATRX):c.2000C>T (p.Pro667Leu) rs61752457
NM_000489.5(ATRX):c.2169G>C (p.Glu723Asp) rs61752456
NM_000489.5(ATRX):c.228G>A (p.Ser76=) rs5959371
NM_000489.5(ATRX):c.2785= (p.Glu929=) rs3088074
NM_000489.5(ATRX):c.3541G>C (p.Val1181Leu) rs61758732
NM_000489.5(ATRX):c.4120+4A>C rs200420513
NM_000489.5(ATRX):c.4365_4367GGA[4] (p.Glu1464del) rs398123423
NM_000489.5(ATRX):c.4483A>T (p.Asn1495Tyr) rs782533736
NM_000489.5(ATRX):c.4635C>A (p.Thr1545=) rs148975763
NM_000489.5(ATRX):c.4659T>C (p.His1553=) rs25641
NM_000489.5(ATRX):c.4699+9C>T rs782140505
NM_000489.5(ATRX):c.4746A>G (p.Thr1582=) rs782097254
NM_000489.5(ATRX):c.4810-19A>G rs1557106791
NM_000489.5(ATRX):c.5271G>A (p.Glu1757=) rs141240580
NM_000489.5(ATRX):c.5697+13A>C rs782387510
NM_000489.5(ATRX):c.5787-24GTTT[4] rs782072699
NM_000489.5(ATRX):c.6405C>T (p.Phe2135=) rs148659669
NM_000489.5(ATRX):c.654A>G (p.Glu218=) rs782378258
NM_000489.5(ATRX):c.7072-8T>C rs782602387
NM_000489.5(ATRX):c.7113G>A (p.Ala2371=) rs782703242
NM_000489.5(ATRX):c.7158A>G (p.Arg2386=) rs1557041056
NM_000489.5(ATRX):c.7233C>T (p.Asn2411=) rs1557034927
NM_000489.5(ATRX):c.846C>T (p.Ser282=) rs148015780

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