ClinVar Miner

List of variants in gene combination RAD51D, RAD51L3-RFFL reported as pathogenic for gastric cancer

Included ClinVar conditions (25):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 13
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_002878.4(RAD51D):c.694C>T (p.Arg232Ter) rs587780104 0.00004
NM_002878.4(RAD51D):c.898C>T (p.Arg300Ter) rs750621215 0.00002
NM_002878.4(RAD51D):c.263+1503C>T rs753486358 0.00001
NM_002878.4(RAD51D):c.144+1dup
NM_002878.4(RAD51D):c.1A>G (p.Met1Val) rs561425038
NM_002878.4(RAD51D):c.263+1617C>T
NM_002878.4(RAD51D):c.270_271dup (p.Lys91fs) rs753862052
NM_002878.4(RAD51D):c.574del (p.Gln192fs)
NM_002878.4(RAD51D):c.746del (p.Asn249fs) rs2091536198
NM_002878.4(RAD51D):c.866del (p.Gly289fs)
NM_002878.4(RAD51D):c.904-2A>T rs1403784434
NM_002878.4(RAD51D):c.941G>A (p.Trp314Ter)
NM_002878.4(RAD51D):c.974del (p.Gly325fs)

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.