Original source

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

T/G | Ancestral: T | Ambiguity code: K | MAF: 0.32 (T)

Chromosome 6:160752914 (forward strand) | View in location tab


with COSMIC COSM3829605 (T/G)

Most severe consequence
Synonymous variant
Evidence status

HGVS names

This variant has 4 HGVS names - Show

Genotyping chips

This variant has assays on 6 chips - Show

About this variant

This variant overlaps 4 transcripts, has 2854 sample genotypes and is mentioned in 3 citations.

Variant displays