ClinVar Miner

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

Submission 1 (benign) minimum review status: Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status: Submission 2 (likely benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 9
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HGVS dbSNP gnomAD frequency
NM_032977.4(CASP10):c.1228G>A (p.Val410Ile) rs13010627 0.04350
NM_032977.4(CASP10):c.1216A>T (p.Ile406Leu) rs80358239 0.00307
NM_032977.4(CASP10):c.1502C>T (p.Pro501Leu) rs148939095 0.00091
NM_032977.4(CASP10):c.347+8C>T rs140246829 0.00056
NM_032977.4(CASP10):c.1347T>C (p.Phe449=) rs147814983 0.00021
NM_032977.4(CASP10):c.930G>T (p.Leu310=) rs149096064 0.00020
NM_032977.4(CASP10):c.1415+8C>G rs200638628 0.00013
NM_032977.4(CASP10):c.923-13T>G rs776612061 0.00001
NM_032977.4(CASP10):c.174C>T (p.Ala58=) rs114625983

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