ClinVar Miner

Variants in gene ATRX with conflicting interpretations "benign" and "uncertain significance"

Submission 1 (benign) minimum review status: Submission 1 (benign) method:
Submission 2 (uncertain significance) minimum review status: Submission 2 (uncertain significance) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 9
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HGVS dbSNP
NM_000489.5(ATRX):c.2656G>C (p.Glu886Gln) rs782374254
NM_000489.5(ATRX):c.3091G>A (p.Gly1031Ser) rs782781078
NM_000489.5(ATRX):c.3395T>C (p.Ile1132Thr) rs587780285
NM_000489.5(ATRX):c.5968T>A (p.Ser1990Thr) rs142180002
NM_000489.5(ATRX):c.831C>T (p.Val277=) rs142561199
NM_000489.6(ATRX):c.118A>G (p.Met40Val)
NM_000489.6(ATRX):c.1648A>G (p.Ser550Gly)
NM_000489.6(ATRX):c.4710T>C rs781829081
NM_000489.6(ATRX):c.5968TCT[2] (p.Ser1992del) rs782391479

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