BRCA1 c.5095_5097delinsAAC ;(p.R1699N)

Variant ID: 17-41215946-CCG-GTT

NM_007294.3(BRCA1):c.5095_5097delinsAAC;(p.R1699N)

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:

Missense Variants of Uncertain Significance: A Powerful Genetic Tool for Function Discovery with Clinical Implications.

Cancers
Sessa, Gaetana G; Ehlén, Åsa Å; von Nicolai, Catharina C; Carreira, Aura A
Publication Date: 2021-07-23

Variant appearance in text: BRCA1: R1699N
PubMed Link: 34359619
Variant Present in the following documents:
  • Main text
  • cancers-13-03719.pdf
View BVdb publication page