MED16 c.863G>A ;(p.R288Q)

Variant ID: 19-885786-C-T

NM_005481.2(MED16):c.863G>A;(p.R288Q)

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:

Whole-exome sequencing identifies somatic mutations and intratumor heterogeneity in inflammatory breast cancer.

Npj Breast Cancer
Luo, Rui R; Chong, Weelic W; Wei, Qiang Q; Zhang, Zhenchao Z; Wang, Chun C; Ye, Zhong Z; Abu-Khalaf, Maysa M MM; Silver, Daniel P DP; Stapp, Robert T RT; Jiang, Wei W; Myers, Ronald E RE; Li, Bingshan B; Cristofanilli, Massimo M; Yang, Hushan H
Publication Date: 2021-06-01

Variant appearance in text: MED16: R288Q
PubMed Link: 34075047
Variant Present in the following documents:
  • 41523_2021_278_MOESM2_ESM.xlsx, sheet 1
View BVdb publication page