Original source

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

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

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


with COSMIC COSM3762526 (C/T)

Most severe consequence
Missense variant
Evidence status


Uniprot VAR_021985

HGVS names

This variant has 3 HGVS names - 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