RARA c.881G>T ;(p.R294L)

Variant ID: 17-38510627-G-T

NM_000964.3(RARA):c.881G>T;(p.R294L)

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:

Clinical Relevance of Genomic Changes in Recurrent Pediatric Solid Tumors.

Translational Oncology
Lee, Boram B; Lee, Ji Won JW; Shim, Joon Ho JH; Joung, Je-Gun JG; Yun, Jae Won JW; Bae, Joon Seol JS; Shin, Hyun-Tae HT; Sung, Ki Woong KW; Park, Woong-Yang WY
Publication Date: 2018-12

Variant appearance in text: RARA: R294L
PubMed Link: 30216764
Variant Present in the following documents:
  • mmc3.xlsx, sheet 1
View BVdb publication page