ClinVar Miner

List of variants reported as uncertain significance for Adenoid cystic carcinoma by Genome Sciences Centre, British Columbia Cancer Agency

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 8
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_000141.5(FGFR2):c.1144T>C (p.Cys382Arg) rs121913474
NM_000215.4(JAK3):c.1765G>A (p.Gly589Ser) rs886039394
NM_003070.5(SMARCA2):c.3638G>C (p.Arg1213Pro) rs1314729940
NM_003073.5(SMARCB1):c.110G>C (p.Arg37Pro) rs398122368
NM_004656.4(BAP1):c.188C>G (p.Ser63Cys) rs747311942
NM_004656.4(BAP1):c.374A>C (p.Glu125Ala) rs1553645926
NM_004991.4(MECOM):c.2200C>T (p.Gln734Ter) rs1553838272
NM_139276.3(STAT3):c.1467T>A (p.Asn489Lys) rs1555564365

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.