MYH7 c.5624T>C ;(p.V1875A)

Variant ID: 14-23883247-A-G

NM_000257.2(MYH7):c.5624T>C;(p.V1875A)

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:

Genetic Variants Are Not Rare in ICD Candidates with Dilated Cardiomyopathy: Time for Next-Generation Sequencing?

Cardiology Research And Practice
Sousa, Alexandra A; Canedo, Paulo P; Campelo, Manuel M; Moura, Brenda B; Leite, Sérgio S; Baixia, Márcia M; Belo, Adriana A; Rocha-Gonçalves, Francisco F; Machado, José Carlos JC; Silva-Cardoso, José J; Martins, Elisabete E; Fatima Investigators,
Publication Date: 2019

Variant appearance in text: MYH7: Val1875Ala
PubMed Link: 31179125
Variant Present in the following documents:
  • Main text
  • CRP2019-2743650.pdf
View BVdb publication page