SLC25A23 c.1071+890C>T

Variant ID: 19-6451433-G-A

NM_024103.2(SLC25A23):c.1071+890C>T

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:

Challenges in whole exome sequencing: an example from hereditary deafness.

Plos One
Sirmaci, Asli A; Edwards, Yvonne J K YJ; Akay, Hatice H; Tekin, Mustafa M
Publication Date: 2012

Variant appearance in text: rs7247153
PubMed Link: 22363784
Variant Present in the following documents:
  • Main text
  • pone.0032000.pdf
View BVdb publication page