Original source

Somatic mutations found in human cancers from the COSMIC project (mapped to GRCh38) (release 71) | View in COSMIC

C/T | Ancestral: C | Ambiguity code: Y

Chromosome 10:50806754 (forward strand) | View in location tab


with COSMIC COSM191229 (C/T) ; dbSNP rs530902814 (C/T)

Most severe consequence
Missense variant
Evidence status

HGVS names

This variant has 16 HGVS names - Show

About this variant

This variant overlaps 9 transcripts and is associated with 2 phenotypes.

Somatic mutation displays