Original source

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


This variation has 5 HGVS names - click the plus to show

This variation has assays on 5 chips - click the plus to show

About this variant

This variant overlaps 10 transcripts, has 2606 individual genotypes and is mentioned in 1 citation.

Variation displays