Original source

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

T/A/G | Ancestral: T | Ambiguity code: D | MAF: 0.20 (G)

Chromosome 12:48145699 (forward strand) | View in location tab


with COSMIC COSM3753261 (T/G), COSM3753260 (T/G)

Most severe consequence
Synonymous variant
Evidence status

HGVS names

This variant has 26 HGVS names - Show

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 56 transcripts and has 3781 sample genotypes.

Variant displays