Original source

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

Alleles
C/G/T | Ambiguity code: B | MAF: < 0.01 (G)
Location

Chromosome 12:52287145 (forward strand) | View in location tab

Co-located

with COSMIC COSM3812304 (C/T) ; HGMD-PUBLIC CM981149 ; PhenCode HIFD_KRT81:c.1204G>A (C/T)

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 14 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_ExomeChip

About this variant

This variant overlaps 10 transcripts, has 2504 individual genotypes and is associated with 4 phenotypes.

Variation displays