CP c.32T>A ;(p.F11Y)

Variant ID: 3-148939548-A-T

NM_000096.3(CP):c.32T>A;(p.F11Y)

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:

Human mitochondrial holocytochrome c synthase's heme binding, maturation determinants, and complex formation with cytochrome c.

Proceedings Of The National Academy Of Sciences Of The United States Of America
San Francisco, Brian B; Bretsnyder, Eric C EC; Kranz, Robert G RG
Publication Date: 2013-02-26

Variant appearance in text: CP: F11Y
PubMed Link: 23150584
Variant Present in the following documents:
  • Main text
View BVdb publication page