ClinVar Miner

Variants in gene CASP10 with conflicting interpretations "likely benign" and "benign"

Submission 1 (likely benign) minimum review status: Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status: Submission 2 (benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 6
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HGVS dbSNP
NM_032977.3(CASP10):c.1347T>C (p.Phe449=) rs147814983
NM_032977.3(CASP10):c.1415+8C>G rs200638628
NM_032977.3(CASP10):c.1502C>T (p.Pro501Leu) rs148939095
NM_032977.3(CASP10):c.174C>T (p.Ala58=) rs114625983
NM_032977.3(CASP10):c.347+8C>T rs140246829
NM_032977.4(CASP10):c.930G>T (p.Leu310=) rs149096064

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