Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.41 (T)
Location

Chromosome 7:155458738 (forward strand) | View in location tab

Co-located

with COSMIC COSM3762526 (C/T)

Most severe consequence
 
Missense variant
Evidence status

Synonyms

Uniprot VAR_021985

This variant has 3 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_ExomeChip

About this variant

This variant overlaps 2 transcripts, has 2775 sample genotypes and is mentioned in 4 citations.

Variant displays