BRCA2 c.1306_1308delinsTTT ;(p.K436F)

Variant ID: 13-32906921-AAG-TTT

NM_000059.3(BRCA2):c.1306_1308delinsTTT;(p.K436F)

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: BRCA2: Lys436Phe
PubMed Link: 35000471
Variant Present in the following documents:
  • sj-pdf-3-imr-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: BRCA2: Lys436Phe
PubMed Link: 35000471
Variant Present in the following documents:
  • sj-pdf-3-imr-10.1177_03000605211070757.pdf
View BVdb publication page