Original source

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

A/C | Ancestral: C | Ambiguity code: M | MAF: 0.22 (C)

Chromosome 8:127416411 (forward strand) | View in location tab


with COSMIC COSM3982388 (A/G), COSM3834038 (A/C), COSM3834039 (A/C), COSM3982389 (A/G)

Most severe consequence
Missense variant
Evidence status


This variant has 3 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 4 transcripts and has 2506 sample genotypes.

Variant displays