Original source

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

C/G/T | Ancestral: G | Ambiguity code: B | MAF: 0.37 (C)

Chromosome 7:87935182 (forward strand) | View in location tab


with COSMIC COSM3750055 (C/G), COSM3750053 (C/G), COSM3750054 (C/G)

Most severe consequence
Missense variant
Evidence status


This variant has 4 synonyms - Show

HGVS names

This variant has 30 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_ExomeChip

About this variant

This variant overlaps 14 transcripts, 1 regulatory feature, has 2882 sample genotypes and is mentioned in 3 citations.

Variant displays