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: 6
Download table as spreadsheet
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

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.