BRCA1 c.4993_4994delinsTC ;(p.V1665S)

Variant ID: 17-41219705-AC-GA

NM_007294.3(BRCA1):c.4993_4994delinsTC;(p.V1665S)

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:

BRCA1 c.4987-3C>G is a pathogenic mutation.

Breast Cancer Research And Treatment
Brandão, Rita D RD; van Roozendaal, Kees E P KE; Tserpelis, Demis D; Caanen, Beppy B; Gómez García, Encarna E; Blok, Marinus J MJ
Publication Date: 2012-01

Variant appearance in text: BRCA1: Val1665Ser
PubMed Link: 22113256
Variant Present in the following documents:
  • Main text
  • 10549_2011_Article_1878.pdf
View BVdb publication page