Original source

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

C/A | Ancestral: A | Ambiguity code: M | MAF: 0.46 (C)

Chromosome 3:52799789 (forward strand) | View in location tab


with COSMIC COSM1617893 (C/A), COSM1617892 (C/A)

Most severe consequence
Missense variant
Evidence status


This variant has 4 synonyms - Show

HGVS names

This variant has 9 HGVS names - Show

Genotyping chips

This variant has assays on 11 chips - Show

About this variant

This variant overlaps 10 transcripts, has 4077 sample genotypes and is mentioned in 1 citation.

Variant displays