CREBBP c.5709G>A ;(p.P1903=)

Variant ID: 16-3779339-C-T

NM_004380.2(CREBBP):c.5709G>A;(p.P1903=)

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: 5709G>A
PubMed Link: 27284491
Variant Present in the following documents:
  • Main text
View BVdb publication page