ClinVar Miner

List of variants in gene ATRX reported as uncertain significance by Ambry Genetics

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Gene type:
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Total variants: 19
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HGVS dbSNP
NM_000489.5(ATRX):c.1041T>G (p.Ile347Met) rs199780997
NM_000489.5(ATRX):c.1183T>G (p.Phe395Val) rs1569539366
NM_000489.5(ATRX):c.1346C>G (p.Pro449Arg)
NM_000489.5(ATRX):c.1694T>C (p.Ile565Thr) rs1557140924
NM_000489.5(ATRX):c.2066A>G (p.Gln689Arg) rs929951326
NM_000489.5(ATRX):c.2304G>C (p.Lys768Asn) rs1557139920
NM_000489.5(ATRX):c.3395T>C (p.Ile1132Thr) rs587780285
NM_000489.5(ATRX):c.3555G>C (p.Lys1185Asn) rs782696086
NM_000489.5(ATRX):c.3913A>C (p.Lys1305Gln) rs782708557
NM_000489.5(ATRX):c.4031A>G (p.Lys1344Arg) rs782556767
NM_000489.5(ATRX):c.4073C>T (p.Thr1358Ile) rs1557124033
NM_000489.5(ATRX):c.5271G>C (p.Glu1757Asp) rs141240580
NM_000489.5(ATRX):c.5311G>C (p.Gly1771Arg) rs1569531574
NM_000489.5(ATRX):c.5540A>T (p.Tyr1847Phe) rs1057521987
NM_000489.5(ATRX):c.5686A>G (p.Lys1896Glu) rs1569528925
NM_000489.5(ATRX):c.6409G>A (p.Ala2137Thr) rs1557060350
NM_000489.5(ATRX):c.6640T>G (p.Leu2214Val)
NM_000489.5(ATRX):c.6887A>G (p.Asn2296Ser) rs782274478
NM_000489.5(ATRX):c.7432C>G (p.Pro2478Ala) rs199543136

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