MYOC c.708C>A ;(p.L236=)

Variant ID: 1-171607759-G-T

NM_000261.1(MYOC):c.708C>A;(p.L236=)

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:

Mitochondrial DNA nucleotide changes in primary congenital glaucoma patients.

Molecular Vision
Kumar, Manoj M; Tanwar, Mukesh M; Faiq, Muneeb Ahmad MA; Pani, Jhumur J; Shamsi, Monis Bilal MB; Dada, Tanuj T; Dada, Rima R
Publication Date: 2013

Variant appearance in text: MYOC: L236L
PubMed Link: 23401651
Variant Present in the following documents:
  • Main text
  • mv-v19-220.pdf
View BVdb publication page