MYBPC3 c.3342C>G ;(p.T1114=)

Variant ID: 11-47354513-G-C

NM_000256.3(MYBPC3):c.3342C>G;(p.T1114=)

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:

Exome sequencing for bipolar disorder points to roles of de novo loss-of-function and protein-altering mutations.

Molecular Psychiatry
Kataoka, M M; Matoba, N N; Sawada, T T; Kazuno, A-A AA; Ishiwata, M M; Fujii, K K; Matsuo, K K; Takata, A A; Kato, T T
Publication Date: 2016-07

Variant appearance in text: MYBPC3: T1114T
PubMed Link: 27217147
Variant Present in the following documents:
  • Main text
  • mp201669x3.xlsx, sheet 1
View BVdb publication page