Original source

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

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

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

Co-located

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

Most severe consequence
Evidence status

This variation has 14 HGVS names - click the plus to show

About this variant

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

Somatic mutation displays