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PC c.382_383delinsCT ;(p.A128L)
Variant ID: 11-66638890-GC-AG
NM_001040716.1(
PC
):c.382_383delinsCT;(p.A128L)
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:
CDKN2A germline alterations and the relevance of genotype-phenotype associations in cancer predisposition.
Hereditary Cancer In Clinical Practice
Chan, Sock Hoai SH; Chiang, Jianbang J; Ngeow, Joanne J
Publication Date: 2021-03-25
Variant appearance in text: PC: Ala128Leu
PubMed Link:
33766116
Variant Present in the following documents:
13053_2021_Article_178.pdf
View BVdb publication page