Original source

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

Alleles
C/G | Ancestral: G | Ambiguity code: S | MAF: 0.37 (C)
Location

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

Co-located

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

Most severe consequence
 
Missense variant
Evidence status

This variant has 4 synonyms - click the plus to show

This variant has 15 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_ExomeChip

About this variant

This variant overlaps 7 transcripts, 1 regulatory feature, has 2882 sample genotypes and is mentioned in 3 citations.

Variant displays