Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.13 (T)
Location

Chromosome 17:40822210 (forward strand) | View in location tab

Co-located

with COSMIC COSM1128722 (C/T) ; PhenCode HIFD_KRT10:c.376G>A (C/T)

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 7 HGVS names - click the plus to show

This variation has assays on 5 chips - click the plus to show

About this variant

This variant overlaps 5 transcripts, has 2505 individual genotypes and is associated with 1 phenotype.

Variation displays