Original source

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

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

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

Co-located

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 - click the plus to show

This variant has 7 HGVS names - click the plus to 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