Original source

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

G/A | Ancestral: G | Ambiguity code: R | MAF: 0.29 (A)

Chromosome 19:10292262 (forward strand) | View in location tab


with COSMIC COSM3742712 (G/A)

Most severe consequence
Missense variant
Evidence status


This variant has 6 synonyms - Show

HGVS names

This variant has 4 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_ExomeChip, Illumina_HumanOmni5

About this variant

This variant overlaps 9 transcripts, 1 regulatory feature, has 2567 sample genotypes and is mentioned in 3 citations.

Variant displays