MUC16 c.6955A>G ;(p.I2319V)

Variant ID: 19-9084860-T-C

NM_024690.2(MUC16):c.6955A>G;(p.I2319V)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Whole exome sequencing of a Saudi family and systems biology analysis identifies CPED1 as a putative causative gene to Celiac Disease.

Saudi Journal Of Biological Sciences
Bokhari, Hifaa A HA; Shaik, Noor Ahmad NA; Banaganapalli, Babajan B; Nasser, Khalidah Khalid KK; Ageel, Hossain Ibrahim HI; Al Shamrani, Ali Saad AS; Rashidi, Omran M OM; Al Ghubayshi, Omar Yaseen OY; Shaik, Jilani J; Ahmad, Aftab A; Alrayes, Nuha Mohammad NM; Al-Aama, Jumana Yousuf JY; Elango, Ramu R; Saadah, Omar Ibrahim OI
Publication Date: 2020-06

Variant appearance in text: MUC16: I2319V; rs200019597
PubMed Link: 32489286
Variant Present in the following documents:
  • Main text
  • main.pdf
View BVdb publication page