Original source

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

A/G | Ancestral: G | Ambiguity code: R | MAF: 0.26 (A)

Chromosome 16:88643420 (forward strand) | View in location tab


with COSMIC COSM3749388 (A/G)

Most severe consequence
Missense variant
Evidence status

Clinical significance


This variant has 6 synonyms - Show

HGVS names

This variant has 6 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_ExomeChip

About this variant

This variant overlaps 13 transcripts, has 2570 sample genotypes, is associated with 1 phenotype and is mentioned in 2 citations.

Variant displays