Original source

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

C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.14 (T)

Chromosome 17:63479839 (forward strand) | View in location tab


with COSMIC COSM4130477 (C/T)

Most severe consequence
Missense variant
Evidence status

HGVS names

This variant has 11 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 11 transcripts, has 2511 sample genotypes and is mentioned in 1 citation.

Variant displays