MYBPC3 c.2332C>T ;(p.P778S)

Variant ID: 11-47359322-G-A

NM_000256.3(MYBPC3):c.2332C>T;(p.P778S)

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:

Molecular analysis of inherited cardiomyopathy using next generation semiconductor sequencing technologies.

Journal Of Translational Medicine
Lu, Chaoxia C; Wu, Wei W; Liu, Fang F; Yang, Kunqi K; Li, Jiacheng J; Liu, Yaping Y; Wang, Rongrong R; Si, Nuo N; Gao, Peng P; Liu, Yongtai Y; Zhang, Shuyang S; Zhang, Xue X
Publication Date: 2018-08-30

Variant appearance in text: MYBPC3: 2332C>T
PubMed Link: 30165862
Variant Present in the following documents:
  • Main text
  • 12967_2018_Article_1605.pdf
View BVdb publication page