Original source

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

C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.13 (T)

Chromosome 4:47406821 (forward strand) | View in location tab


with COSMIC COSM3760643 (C/T)

Most severe consequence
Synonymous variant
Evidence status


Archive dbSNP rs57787234, rs17600630

HGVS names

This variant has 3 HGVS names - Show

Genotyping chips

This variant has assays on 11 chips - Show

About this variant

This variant overlaps 2 transcripts, has 3792 sample genotypes and is mentioned in 2 citations.

Variant displays