Original source

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

G/T | Ancestral: G | Ambiguity code: K | MAF: 0.18 (T)

Chromosome 5:135029306 (forward strand) | View in location tab


with COSMIC COSM3760919 (G/T)

Most severe consequence
Synonymous variant
Evidence status

HGVS names

This variant has 8 HGVS names - Show

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 9 transcripts, 1 regulatory feature, has 3526 sample genotypes and is mentioned in 1 citation.

Variant displays