BRCA2 c.5490C>A ;(p.S1830=)

Variant ID: 13-32913982-C-A

NM_000059.3(BRCA2):c.5490C>A;(p.S1830=)

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:

Prevalance of BRCA1 and BRCA2 mutations in familial breast cancer patients in Lebanon.

Hereditary Cancer In Clinical Practice
Jalkh, Nadine N; Nassar-Slaba, Jinane J; Chouery, Eliane E; Salem, Nabiha N; Uhrchammer, Nancy N; Golmard, Lisa L; Stoppa-Lyonnet, Domique D; Bignon, Yves-Jean YJ; Mégarbané, André A
Publication Date: 2012-06-19

Variant appearance in text: BRCA2: S1830S
PubMed Link: 22713736
Variant Present in the following documents:
  • Main text
  • 1897-4287-10-7.pdf
View BVdb publication page