RET c.487C>G ;(p.R163G)

Variant ID: 10-43597939-C-G

NM_020975.4(RET):c.487C>G;(p.R163G)

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:

RTK-RAS pathway mutation is enriched in myeloid sarcoma.

Blood Cancer Journal
Choi, Mihong M; Jeon, Yoon Kyung YK; Sun, Choong-Hyun CH; Yun, Hong-Seok HS; Hong, Junshik J; Shin, Dong-Yeop DY; Kim, Inho I; Yoon, Sung-Soo SS; Koh, Youngil Y
Publication Date: 2018-05-23

Variant appearance in text: RET: 487C>G
PubMed Link: 29789584
Variant Present in the following documents:
  • Main text
View BVdb publication page