Original source

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

T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.05 (C)

Chromosome 15:71812093 (forward strand) | View in location tab


with COSMIC COSM3754455 (T/C), COSM3754456 (T/C), COSM3754454 (T/C)

Most severe consequence
Missense variant
Evidence status

Clinical significance


This variant has 2 synonyms - Show

HGVS names

This variant has 7 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_ExomeChip

About this variant

This variant overlaps 3 transcripts, has 2506 sample genotypes and is associated with 1 phenotype.

Variant displays