NAT1 c.110T>G ;(p.F37C)

Variant ID: 8-18079666-T-G

NM_000662.5(NAT1):c.110T>G;(p.F37C)

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:

Diseases Caused by Mutations in Mitochondrial Carrier Genes SLC25: A Review.

Biomolecules
Palmieri, Ferdinando F; Scarcia, Pasquale P; Monné, Magnus M
Publication Date: 2020-04-23

Variant appearance in text: AAC1: 110T>G
PubMed Link: 32340404
Variant Present in the following documents:
  • biomolecules-10-00655-s001.pdf
View BVdb publication page