Original source

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

C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.40 (C)

Chromosome 4:54100500 (forward strand) | View in location tab


with COSMIC COSM3760660 (C/T)

Most severe consequence
Synonymous variant
Evidence status

HGVS names

This variant has 9 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo

About this variant

This variant overlaps 6 transcripts and has 3690 sample genotypes.

Variant displays