Original source

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

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

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

Co-located

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

Most severe consequence
Evidence status

This variation has 16 HGVS names - click the plus to show

About this variant

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

Somatic mutation displays