MYOC c.423C>A ;(p.A141=)

Variant ID: 1-171621329-G-T

NM_000261.1(MYOC):c.423C>A;(p.A141=)

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:

Screening of CYP1B1 and MYOC in Moroccan families with primary congenital glaucoma: three novel mutations in CYP1B1.

Molecular Vision
Hilal, Latifa L; Boutayeb, Soraya S; Serrou, Aziza A; Refass-Buret, Loubna L; Shisseh, Hafsa H; Bencherifa, Fatiha F; El Mzibri, Mohammed M; Benazzouz, Bouchra B; Berraho, Amina A
Publication Date: 2010-07-02

Variant appearance in text: MYOC: A141A
PubMed Link: 20664688
Variant Present in the following documents:
  • Main text
  • mv-v16-1215.pdf
View BVdb publication page