MSH6 c.1717T>C ;(p.F573L)

Variant ID: 2-48026839-T-C

NM_000179.2(MSH6):c.1717T>C;(p.F573L)

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:

Mutational dynamics of early and late relapsed childhood ALL: rapid clonal expansion and long-term dormancy.

Blood Advances
Spinella, Jean-François JF; Richer, Chantal C; Cassart, Pauline P; Ouimet, Manon M; Healy, Jasmine J; Sinnett, Daniel D
Publication Date: 2018-02-13

Variant appearance in text: MSH6: F573L
PubMed Link: 29365312
Variant Present in the following documents:
  • Main text
View BVdb publication page