Original source

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

C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.34 (T)

Chromosome 6:159907588 (forward strand) | View in location tab


with COSMIC COSM3761631 (C/T)

Most severe consequence
Synonymous variant
Evidence status


Archive dbSNP rs58693554, rs57966069

HGVS names

This variant has 3 HGVS names - Show

Genotyping chips

This variant has assays on 7 chips - Show

About this variant

This variant overlaps 1 transcript, has 4072 sample genotypes and is mentioned in 2 citations.

Variant displays