Original source

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

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

Chromosome 10:16890385 (forward strand) | View in location tab


with COSMIC COSM32707 (G/A)

Most severe consequence
Missense variant
Evidence status


Uniprot VAR_035831

HGVS names

This variant has 6 HGVS names - Show

Genotyping chips

This variant has assays on: HumanCoreExome-12, Illumina_ExomeChip, Illumina_HumanOmni5

About this variant

This variant overlaps 2 transcripts, has 2505 sample genotypes and is associated with 1 phenotype.

Variant displays