Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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


This variant has 3 HGVS names - click the plus to show

This variant has assays on 6 chips - click the plus to show

About this variant

This variant overlaps 4 transcripts, has 2546 sample genotypes and is mentioned in 3 citations.

Variant displays