CREBBP c.2917C>A ;(p.P973T)

Variant ID: 16-3819318-G-T

NM_004380.2(CREBBP):c.2917C>A;(p.P973T)

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:

Whole‑exome sequencing analysis of products of conception identifies novel mutations associated with missed abortion.

Molecular Medicine Reports
Fu, Meng M; Mu, Sha S; Wen, Chunyan C; Jiang, Shufang S; Li, Lin L; Meng, Yuanguang Y; Peng, Hongmei H
Publication Date: 2018-08

Variant appearance in text: CREBBP: 2917C>A; P973T
PubMed Link: 29956774
Variant Present in the following documents:
  • Main text
  • mmr-18-02-2027.pdf
View BVdb publication page