Original source

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

C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.10 (T)

Chromosome 6:22287516 (forward strand) | View in location tab


with COSMIC COSM4003818 (C/T)

Most severe consequence
Synonymous variant
Evidence status

HGVS names

This variant has 8 HGVS names - Show

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 4 transcripts, has 3683 sample genotypes and is mentioned in 3 citations.

Variant displays