Original source

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

A/G | Ancestral: G | Ambiguity code: R | MAF: 0.45 (A)

Chromosome 15:74035775 (forward strand) | View in location tab


with COSMIC COSM3754464 (A/G)

Most severe consequence
Missense variant
Evidence status


This variant has 18 HGVS names - click the plus to show

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

About this variant

This variant overlaps 20 transcripts and has 3255 sample genotypes.

Variant displays