Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

C/A | Ancestral: C | Ambiguity code: M | MAF: 0.47 (C)

Chromosome 9:286593 (forward strand) | View in location tab


with COSMIC COSM3763875 (C/A), COSM3763874 (C/A)

Most severe consequence
Missense variant
Evidence status

Clinical significance


This variant has 6 synonyms - Show

HGVS names

This variant has 22 HGVS names - Show

Genotyping chips

This variant has assays on 11 chips - Show

About this variant

This variant overlaps 13 transcripts, has 4165 sample genotypes and is associated with 1 phenotype.

Variant displays