Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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

This variant has 2 HGVS names - click the plus to show

This variant has assays on 11 chips - click the plus to show

About this variant

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

Variant displays