SI c.1301_1302delinsAT ;(p.R434H)

Variant ID: 3-164776847-TC-AT

NM_001041.3(SI):c.1301_1302delinsAT;(p.R434H)

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:

Recurrent high-impact mutations at cognate structural positions in class A G protein-coupled receptors expressed in tumors.

Proceedings Of The National Academy Of Sciences Of The United States Of America
Huh, Eunna E; Gallion, Jonathan J; Agosto, Melina A MA; Wright, Sara J SJ; Wensel, Theodore G TG; Lichtarge, Olivier O
Publication Date: 2021-12-21

Variant appearance in text: SI: R434H
PubMed Link: 34916293
Variant Present in the following documents:
  • pnas.2113373118.sapp.pdf
View BVdb publication page