RHOA c.502_503delinsCA ;(p.R168Q)

Variant ID: 3-49397721-CT-TG

NM_001664.2(RHOA):c.502_503delinsCA;(p.R168Q)

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:

Unsupervised detection of cancer driver mutations with parsimony-guided learning.

Nature Genetics
Kumar, Runjun D RD; Swamidass, S Joshua SJ; Bose, Ron R
Publication Date: 2016-10

Variant appearance in text: RHOA: R168Q
PubMed Link: 27618449
Variant Present in the following documents:
  • Main text
View BVdb publication page