Original source

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

G/A/T | Ancestral: G | Ambiguity code: D | MAF: 0.01 (T)

Chromosome 15:74720646 (forward strand) | View in location tab


with COSMIC COSM3754467 (G/T) ; HGMD-PUBLIC CM057662

Most severe consequence
Missense variant
Evidence status


This variant has 6 synonyms - Show

HGVS names

This variant has 26 HGVS names - Show

Genotyping chips

This variant has assays on 7 chips - Show

About this variant

This variant overlaps 20 transcripts, has 2888 sample genotypes and is mentioned in 17 citations.

Variant displays