TLN2 c.5061G>C ;(p.Q1687H)

Variant ID: 15-63055861-G-C

NM_015059.2(TLN2):c.5061G>C;(p.Q1687H)

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:

A high definition picture of somatic mutations in chronic lymphoproliferative disorder of natural killer cells.

Blood Cancer Journal
Gasparini, Vanessa Rebecca VR; Binatti, Andrea A; Coppe, Alessandro A; Teramo, Antonella A; Vicenzetto, Cristina C; Calabretto, Giulia G; Barilà, Gregorio G; Barizza, Annica A; Giussani, Edoardo E; Facco, Monica M; Mustjoki, Satu S; Semenzato, Gianpietro G; Zambello, Renato R; Bortoluzzi, Stefania S
Publication Date: 2020-04-22

Variant appearance in text: TLN2: Gln1687His
PubMed Link: 32321919
Variant Present in the following documents:
  • 41408_2020_309_MOESM4_ESM.pdf
View BVdb publication page