ClinVar Miner

List of variants in gene ATRX reported as likely benign for History of neurodevelopmental disorder

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Gene type:
ClinVar version:
Total variants: 19
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HGVS dbSNP
NM_000489.5(ATRX):c.1168C>T (p.Arg390Cys)
NM_000489.5(ATRX):c.1290A>G (p.Lys430=) rs1569539312
NM_000489.5(ATRX):c.12G>A (p.Glu4=) rs782765957
NM_000489.5(ATRX):c.2650G>A (p.Glu884Lys) rs200343648
NM_000489.5(ATRX):c.2720G>A (p.Arg907Gln) rs143413618
NM_000489.5(ATRX):c.2922C>T (p.Ser974=) rs1476227727
NM_000489.5(ATRX):c.3152A>G (p.Asp1051Gly) rs1557138081
NM_000489.5(ATRX):c.3211G>A (p.Gly1071Arg) rs143621153
NM_000489.5(ATRX):c.4035G>A (p.Leu1345=) rs111725949
NM_000489.5(ATRX):c.4047C>T (p.Asp1349=)
NM_000489.5(ATRX):c.4130A>G (p.Glu1377Gly) rs782553301
NM_000489.5(ATRX):c.4239A>G (p.Glu1413=) rs141974120
NM_000489.5(ATRX):c.4275G>A (p.Arg1425=) rs1569535653
NM_000489.5(ATRX):c.4810-3T>C
NM_000489.5(ATRX):c.5349A>G (p.Pro1783=)
NM_000489.5(ATRX):c.570T>G (p.Pro190=) rs188831993
NM_000489.5(ATRX):c.6489T>C (p.Tyr2163=)
NM_000489.5(ATRX):c.6869A>G (p.Asn2290Ser) rs368498507
NM_000489.5(ATRX):c.7083C>T (p.Asn2361=) rs3027525

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