CREBBP c.932C>A ;(p.P311H)

Variant ID: 16-3860647-G-T

NM_004380.2(CREBBP):c.932C>A;(p.P311H)

This variant was identified in 1 publication

View GRCh38 version.




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: 932C>A; P311H
PubMed Link: 27284491
Variant Present in the following documents:
  • Main text
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