Original source

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

G/A | Ancestral: G | Ambiguity code: R | MAF: 0.22 (G)

Chromosome 10:69382664 (forward strand) | View in location tab


with COSMIC COSM4144803 (G/A), COSM4144805 (G/A), COSM4144804 (G/A), COSM4144806 (G/A)

Most severe consequence
Synonymous variant
Evidence status


Archive dbSNP rs17850368, rs60876495

HGVS names

This variant has 13 HGVS names - Show

Genotyping chips

This variant has assays on 10 chips - Show

About this variant

This variant overlaps 6 transcripts, 1 regulatory feature, has 3806 sample genotypes and is mentioned in 4 citations.

Variant displays