Original source

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

C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.11 (T)

Chromosome 22:21031696 (forward strand) | View in location tab


with COSMIC COSM4135195 (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: Illumina_HumanOmni1-Quad, Illumina_HumanOmni5

About this variant

This variant overlaps 11 transcripts and has 2540 sample genotypes.

Variant displays