ClinVar Miner

List of variants in gene ATRX reported as uncertain significance by GeneDx

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Gene type:
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Total variants: 32
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HGVS dbSNP
NM_000489.5(ATRX):c.1033G>A (p.Ala345Thr) rs149249195
NM_000489.5(ATRX):c.1169G>A (p.Arg390His) rs367986587
NM_000489.5(ATRX):c.1236C>A (p.Asp412Glu) rs951634317
NM_000489.5(ATRX):c.1252C>G (p.Arg418Gly) rs1057523785
NM_000489.5(ATRX):c.1478A>G (p.His493Arg) rs947189709
NM_000489.5(ATRX):c.1608G>T (p.Met536Ile) rs1057518436
NM_000489.5(ATRX):c.2066A>G (p.Gln689Arg) rs929951326
NM_000489.5(ATRX):c.2461_2466del (p.Leu821_Glu822del) rs781862926
NM_000489.5(ATRX):c.259A>G (p.Thr87Ala) rs1557150036
NM_000489.5(ATRX):c.2617G>C (p.Glu873Gln) rs967071645
NM_000489.5(ATRX):c.2680A>C (p.Thr894Pro) rs145807475
NM_000489.5(ATRX):c.278A>T (p.Asp93Val) rs1064796774
NM_000489.5(ATRX):c.2875G>T (p.Asp959Tyr) rs1057523431
NM_000489.5(ATRX):c.3224A>G (p.Asp1075Gly) rs1064796745
NM_000489.5(ATRX):c.3495_3500del (p.Asn1165_Lys1166del) rs1557137281
NM_000489.5(ATRX):c.3655G>A (p.Gly1219Arg) rs1057524797
NM_000489.5(ATRX):c.3670C>G (p.Gln1224Glu) rs1057522687
NM_000489.5(ATRX):c.4070A>G (p.Lys1357Arg) rs1064796812
NM_000489.5(ATRX):c.4312A>G (p.Asn1438Asp) rs971839925
NM_000489.5(ATRX):c.4905G>T (p.Met1635Ile) rs1045875195
NM_000489.5(ATRX):c.5087_5089dup (p.Lys1696dup) rs1557106446
NM_000489.5(ATRX):c.5212A>G (p.Ile1738Val) rs1057523890
NM_000489.5(ATRX):c.5540A>T (p.Tyr1847Phe) rs1057521987
NM_000489.5(ATRX):c.5722G>T (p.Asp1908Tyr) rs1057522290
NM_000489.5(ATRX):c.6097A>G (p.Ile2033Val) rs1057521636
NM_000489.5(ATRX):c.6202C>T (p.Pro2068Ser) rs1557079194
NM_000489.5(ATRX):c.631C>T (p.Arg211Cys) rs782241890
NM_000489.5(ATRX):c.6464G>A (p.Gly2155Glu) rs1057518599
NM_000489.5(ATRX):c.7141G>A (p.Glu2381Lys) rs1557041077
NM_000489.5(ATRX):c.7334T>A (p.Ile2445Asn) rs1057520923
NM_000489.5(ATRX):c.847G>A (p.Val283Ile) rs1057522580
NM_000489.5(ATRX):c.884_886AGA[2] (p.Lys297del) rs1064795918

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