CIViC Compass
Research use only — not FDA-cleared, not medical advice. Always consult FDA-approved labeling and a qualified clinician.

BRCA2

CIViC ID: 7 · Entrez: 675

Aliases: BRCC2,BROVCA2,FACD,FAD,FAD1,FANCD,FANCD1,GLM3,PNCA2,XRCC11,BRCA2

Description

BRCA2 mutations in the germline have become a hallmark for hereditary breast and ovarian cancers. Variants that have been demonstrated to reduce the function of the protein have been shown to increase the risk for these cancers, as well as prostate and pancreatic cancer. These findings have been the impetus for the increased popularity of genetic testing of healthy individuals to assess risk. Recent studies in ovarian cancer have also demonstrated that BRCA mutation status can predict treatment response. A number of trials assessing BRCA mutation status have shown an improved response to platinum agents, and more recently has led to the FDA-approval of PARP inhibitors for BRCA-positive ovarian cancers. These studies have resulted in the Society of Gynecologic Oncology to recommend germline BRCA testing in all patients with a diagnosis of ovarian cancer.

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Variants (11)

CIViC IDNameHGVSType(s)
661D3095E
ASP3095GLU,RS80359198
NM_000059.3:c.9285C>A,NP_000050.2:p.Asp3095Glu,ENST00000544455.1:c.9285C>A,NC_000013.10:g.32968854C>Amissense_variant
2871K3326*
132Loss-of-functionloss_of_function_variant
1248M1I
MET1ILE,RS80358650
NC_000013.10:g.32890600G>T,NM_000059.3:c.3G>T,NP_000050.2:p.Met1Ile,ENST00000544455.1:c.3G>Tmissense_variant
1247M1R
MET1ARG,RS80358547
NM_000059.3:c.2T>G,NC_000013.10:g.32890599T>G,NP_000050.2:p.Met1Arg,ENST00000544455.1:c.2T>Gmissense_variant
186Mutationgene_variant,loss_of_function_variant
1252R2336P
ARG2336PRO,RS28897743
NM_000059.3:c.7007G>C,NP_000050.2:p.Arg2336Pro,NC_000013.10:g.32921033G>C,ENST00000544455.1:c.7007G>Cmissense_variant
708TRUNCATING MUTATIONfeature_truncation
1249V159M
VAL159MET,RS80358702
ENST00000544455.1:c.475G>A,NM_000059.3:c.475G>A,NP_000050.2:p.Val159Met,NC_000013.10:g.32900287G>Amissense_variant
1251V211INC_000013.10:g.32900751G>Amissense_variant
1250V211LNC_000013.10:g.32900751G>Cmissense_variant