Original source

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

G/A | Ancestral: G | Ambiguity code: R | MAF: 0.07 (A)

Chromosome 11:101583461 (forward strand) | View in location tab


with COSMIC COSM3752082 (G/A)

Most severe consequence
Missense variant
Evidence status

This variant has 10 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_ExomeChip

About this variant

This variant overlaps 6 transcripts, 1 regulatory feature, has 2505 sample genotypes and is mentioned in 4 citations.

Variant displays