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

Variant ID: 1-171607759-G-A

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

This variant was identified in 3 publications

View GRCh38 version.




Publications:


A pan-cancer analysis of synonymous mutations.

Nature Communications
Sharma, Yogita Y; Miladi, Milad M; Dukare, Sandeep S; Boulay, Karine K; Caudron-Herger, Maiwen M; Groß, Matthias M; Backofen, Rolf R; Diederichs, Sven S
Publication Date: 2019-06-12

Variant appearance in text: MYOC: 708C>T
PubMed Link: 31189880
Variant Present in the following documents:
  • 41467_2019_10489_MOESM7_ESM.xlsx, sheet 1
View BVdb publication page



Comprehensive genomic analysis of Oesophageal Squamous Cell Carcinoma reveals clinical relevance.

Scientific Reports
Du, Peina P; Huang, Peide P; Huang, Xuanlin X; Li, Xiangchun X; Feng, Zhimin Z; Li, Fengyu F; Liang, Shaoguang S; Song, Yongmei Y; Stenvang, Jan J; Brünner, Nils N; Yang, Huanming H; Ou, Yunwei Y; Gao, Qiang Q; Li, Lin L
Publication Date: 2017-11-10

Variant appearance in text: MYOC: 708C>T; L236L
PubMed Link: 29127303
Variant Present in the following documents:
  • 41598_2017_14909_MOESM4_ESM.xlsx, sheet 1
View BVdb publication page



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