Bibliome.ai browser hg19
Search
About
Stats
FAQ
CREBBP c.1310G>C ;(p.S437T)
Variant ID: 16-3842002-C-G
NM_004380.2(
CREBBP
):c.1310G>C;(p.S437T)
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:
Mutation profiles of synchronous colorectal cancers from a patient with Lynch syndrome suggest distinct oncogenic pathways.
Journal Of Gastrointestinal Oncology
Wheeler, Scott R SR; Shi, Chanjuan C; Holt, Jonathan A JA; Vnencak-Jones, Cindy L CL
Publication Date: 2016-06
Variant appearance in text: CREBBP: 1310G>C; S437T
PubMed Link:
27284491
Variant Present in the following documents:
Main text
View BVdb publication page