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BRCA2 c.1795_1796delinsGG ;(p.S599G)
Variant ID: 13-32907410-TC-GG
NM_000059.3(
BRCA2
):c.1795_1796delinsGG;(p.S599G)
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:
Androgen receptor signaling and mutations in prostate cancer.
Asian Journal Of Andrology
Koochekpour, Shahriar S
Publication Date: 2010-09
Variant appearance in text: BRCA2: S599G
PubMed Link:
20711217
Variant Present in the following documents:
Main text
View BVdb publication page