Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [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
Evidence status


This variation has 8 HGVS names - click the plus to show

Genotyping chips

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

About this variant

This variant overlaps 11 transcripts, has 1103 individual genotypes and is mentioned in 1 citation.

Variation displays