Original source

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

T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.02 (C)

Chromosome 15:63059674 (forward strand) | View in location tab


with COSMIC COSM3754394 (T/C), COSM3754392 (T/C), COSM3754395 (T/C), COSM3754393 (T/C), COSM3754391 (T/C)

Most severe consequence
Synonymous variant
Evidence status

Clinical significance


This variant has 2 synonyms - Show

HGVS names

This variant has 43 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Cardio-Metabo_Chip, Illumina_HumanOmni2.5, Illumina_HumanOmni5

About this variant

This variant overlaps 32 transcripts, has 2504 sample genotypes, is associated with 2 phenotypes and is mentioned in 2 citations.

Variant displays