Original source

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

C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.04 (T)

Chromosome 13:51946335 (forward strand) | View in location tab


with COSMIC COSM432488 (C/T)

Most severe consequence
Synonymous variant
Evidence status

Clinical significance


This variant has 2 synonyms - Show

HGVS names

This variant has 14 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5

About this variant

This variant overlaps 8 transcripts, has 2901 sample genotypes, is associated with 2 phenotypes and is mentioned in 4 citations.

Variant displays