Bibliome.ai browser hg19
Search
About
Stats
FAQ
PALB2 c.3497G>T ;(p.G1166V)
Variant ID: 16-23614844-C-A
NM_024675.3(
PALB2
):c.3497G>T;(p.G1166V)
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:
Functional characterization of 84 PALB2 variants of uncertain significance.
Genetics In Medicine : Official Journal Of The American College Of Medical Genetics
Wiltshire, Timothy T; Ducy, Mandy M; Foo, Tzeh Keong TK; Hu, Chunling C; Lee, Kun Y KY; Belur Nagaraj, Anil A; Rodrigue, Amélie A; Gomes, Thiago T TT; Simard, Jacques J; Monteiro, Alvaro N A ANA; Xia, Bing B; Carvalho, Marcelo A MA; Masson, Jean-Yves JY; Couch, Fergus J FJ
Publication Date: 2020-03
Variant appearance in text: PALB2: G1166V
PubMed Link:
31636395
Variant Present in the following documents:
Main text
41436_2019_Article_682.pdf
View BVdb publication page