Original source

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

C/A | Ancestral: C | Ambiguity code: M

Chromosome 1:86903328 (forward strand) | View in location tab


with COSMIC COSM1627232 (C/A), COSM1627233 (C/A)

Most severe consequence
Missense variant
Evidence status

HGVS names

This variant has 15 HGVS names - Show

About this variant

This variant overlaps 8 transcripts and is associated with 1 phenotype.

Somatic mutation displays