Original source

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

G/T | Ancestral: G | Ambiguity code: K | MAF: 0.35 (T)

Chromosome 15:74035800 (forward strand) | View in location tab


with COSMIC COSM3773731 (G/T)

Most severe consequence
Missense variant
Evidence status


This variant has 18 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 20 transcripts and has 2513 sample genotypes.

Variant displays