MYOC c.879G>C ;(p.T293=)

Variant ID: 1-171605701-C-G

NM_000261.1(MYOC):c.879G>C;(p.T293=)

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:

Low prevalence of myocilin mutations in an African American population with primary open-angle glaucoma.

Molecular Vision
Liu, Wenjing W; Liu, Yutao Y; Challa, Pratap P; Herndon, Leon W LW; Wiggs, Janey L JL; Girkin, Christopher A CA; Allingham, R Rand RR; Hauser, Michael A MA
Publication Date: 2012

Variant appearance in text: MYOC: Thr293Thr
PubMed Link: 22933836
Variant Present in the following documents:
  • Main text
  • mv-v18-2241.pdf
View BVdb publication page