MED16 c.187C>T ;(p.H63Y)

Variant ID: 19-890227-G-A

NM_005481.2(MED16):c.187C>T;(p.H63Y)

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:

Elucidating the pathogenesis of synchronous and metachronous tumors in a woman with endometrioid carcinomas using a whole-exome sequencing approach.

Cold Spring Harbor Molecular Case Studies
Wu, Ren-Chin RC; Veras, Ema E; Lin, Jeffrey J; Gerry, Emily E; Bahadirli-Talbott, Asli A; Baras, Alexander A; Ayhan, Ayse A; Shih, Ie-Ming IM; Wang, Tian-Li TL
Publication Date: 2017-11

Variant appearance in text: MED16: 187C>T; H63Y
PubMed Link: 29162652
Variant Present in the following documents:
  • supp_mcs.a001693_Supplemental_Table_2.xlsx, sheet 1
View BVdb publication page