RARA c.1154_1155insTTGTC ;(p.S386Cfs*12)

Variant ID: 17-38511656-G-GTTGTC

NM_000964.3(RARA):c.1154_1155insTTGTC;(p.S386Cfs*12)

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:

t(15; 17) associated with primary myelofibrosis: a case report of an unusual clinical presentation and diagnostic dilemma.

Oncotargets And Therapy
Nadiminti, Kalyan K; Silverman, Margarida M; Bhagavathi, Sharathkumar S; Vikas, Praveen P
Publication Date: 2019

Variant appearance in text: RARA: 1154_1155insTTGTC
PubMed Link: 31371984
Variant Present in the following documents:
  • Main text
  • ott-12-5449.pdf
View BVdb publication page