Original source

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

G/T | Ancestral: G | Ambiguity code: K | MAF: 0.39 (T)

Chromosome 16:3254573 (forward strand) | View in location tab


with COSMIC COSM1128970 (G/T)

Most severe consequence
Synonymous variant
Evidence status

Clinical significance


This variant has 3 synonyms - Show

HGVS names

This variant has 23 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni1-Quad, Illumina_HumanOmni5

About this variant

This variant overlaps 15 transcripts, has 2557 sample genotypes, is associated with 1 phenotype and is mentioned in 2 citations.

Variant displays