Bibliome.ai browser hg19
Search
About
Stats
FAQ
MYBPC3 c.1664T>C ;(p.M555T)
Variant ID: 11-47363668-A-G
NM_000256.3(
MYBPC3
):c.1664T>C;(p.M555T)
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:
Coding sequence rare variants identified in MYBPC3, MYH6, TPM1, TNNC1, and TNNI3 from 312 patients with familial or idiopathic dilated cardiomyopathy.
Circulation. Cardiovascular Genetics
Hershberger, Ray E RE; Norton, Nadine N; Morales, Ana A; Li, Duanxiang D; Siegfried, Jill D JD; Gonzalez-Quintana, Jorge J
Publication Date: 2010-04
Variant appearance in text: MYBPC3: Met555Thr
PubMed Link:
20215591
Variant Present in the following documents:
Main text
View BVdb publication page