Original source

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

T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.29 (T)

Chromosome 9:114790605 (forward strand) | View in location tab


with COSMIC COSM3763572 (T/C), COSM3982713 (T/C)

Most severe consequence
Synonymous variant
Evidence status


Archive dbSNP rs59393366

HGVS names

This variant has 5 HGVS names - Show

Genotyping chips

This variant has assays on 9 chips - Show

About this variant

This variant overlaps 2 transcripts, 1 regulatory feature, has 4070 sample genotypes, is associated with 2 phenotypes and is mentioned in 18 citations.

Variant displays