BRCA1 c.5223_5226del ;(p.N1742Efs*22)

Variant ID: 17-41209119-CATTG-C

NM_007294.3(BRCA1):c.5223_5226del;(p.N1742Efs*22)

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/BRCA2 mutation spectrum analysis in South Asia: a systematic review.

The Journal Of International Medical Research
Kharel, Sanjeev S; Shrestha, Suraj S; Yadav, Siddhartha S; Shakya, Prafulla P; Baidya, Sujita S; Hirachan, Suzita S
Publication Date: 2022-01

Variant appearance in text: BRCA1: 5222_5225del
PubMed Link: 35000471
Variant Present in the following documents:
  • Main text
  • 10.1177_03000605211070757.pdf
View BVdb publication page


BRCA1/BRCA2 mutation spectrum analysis in South Asia: a systematic review.

The Journal Of International Medical Research
Kharel, Sanjeev S; Shrestha, Suraj S; Yadav, Siddhartha S; Shakya, Prafulla P; Baidya, Sujita S; Hirachan, Suzita S
Publication Date: 2022-01

Variant appearance in text: BRCA1: 5222_5225del
PubMed Link: 35000471
Variant Present in the following documents:
  • Main text
  • 10.1177_03000605211070757.pdf
View BVdb publication page