Original source

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

G/A | Ancestral: G | Ambiguity code: R | MAF: 0.44 (A)

Chromosome 19:844020 (forward strand) | View in location tab


with COSMIC COSM3723224 (G/A)

Most severe consequence
Missense variant
Evidence status


This variant has 7 synonyms - Show

HGVS names

This variant has 5 HGVS names - Show

Genotyping chips

This variant has assays on 11 chips - Show

About this variant

This variant overlaps 2 transcripts, 1 regulatory feature, has 3689 sample genotypes and is mentioned in 1 citation.

Variant displays