BRCA2 c.1797T>G ;(p.S599=)

Variant ID: 13-32907412-T-G

NM_000059.3(BRCA2):c.1797T>G;(p.S599=)

This variant was identified in 1 publication

View GRCh38 version.



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

Publications:

Identification of the most common BRCA alterations through analysis of germline mutation databases: Is droplet digital PCR an additional strategy for the assessment of such alterations in breast and ovarian cancer families?

International Journal Of Oncology
Lavoro, Alessandro A; Scalisi, Aurora A; Candido, Saverio S; Zanghì, Guido Nicola GN; Rizzo, Roberta R; Gattuso, Giuseppe G; Caruso, Giuseppe G; Libra, Massimo M; Falzone, Luca L
Publication Date: 2022-05

Variant appearance in text: BRCA2: Ser599=
PubMed Link: 35383859
Variant Present in the following documents:
  • ijo-60-05-05349.pdf
View BVdb publication page