ClinVar Miner

List of variants in gene CASP10 studied for cancer

Included ClinVar conditions (474):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 5
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_032977.4(CASP10):c.259C>T (p.Arg87Trp) rs551818122 0.00013
NM_032977.4(CASP10):c.922+5G>A rs559244194 0.00011
NM_032977.4(CASP10):c.440T>C (p.Met147Thr) rs121909776 0.00003
NM_032977.4(CASP10):c.1271C>T (p.Thr424Ile) rs1559309649
NM_032977.4(CASP10):c.769C>T (p.Gln257Ter) rs121909775

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.