KMT2C c.14303A>G ;(p.E4768G)

Variant ID: 7-151841838-T-C

NM_170606.2(KMT2C):c.14303A>G;(p.E4768G)

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:

Utility of exome sequencing in routine care for metastatic colorectal cancer.

Molecular And Clinical Oncology
D'Agay, Melchior De Giraud MG; Galland, Loïck L; Tharin, Zoe Z; Truntzer, Caroline C; Ghiringhelli, Francois F
Publication Date: 2021-11

Variant appearance in text: KMT2C: 14303A>G; Glu4768Gly
PubMed Link: 34631054
Variant Present in the following documents:
  • Supplementary_Data.pdf
View BVdb publication page