Bibliome.ai browser hg19
Search
About
Stats
FAQ
APC c.1385A>G ;(p.H462R)
Variant ID: 5-112157665-A-G
NM_000038.5(
APC
):c.1385A>G;(p.H462R)
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:
Rare germline variants in DNA repair-related genes are accountable for papillary thyroid cancer susceptibility.
Endocrine
Mio, Catia C; Verrienti, Antonella A; Pecce, Valeria V; Sponziello, Marialuisa M; Damante, Giuseppe G
Publication Date: 2021-09
Variant appearance in text: APC: 1385A>G
PubMed Link:
33821390
Variant Present in the following documents:
12020_2021_Article_2705.pdf
View BVdb publication page