Original source

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

G/T|Ancestral: G|Ambiguity code: K

Chromosome 12:52306272 (forward strand)|View in location tab

Co-located variants

HGMD-PUBLIC CM970852 ; PhenCode HIFD_KRT86:c.1239G>T (G/T)

Most severe consequence
Missense variant
Evidence status

Clinical significance


This variant has 3 synonyms - Show

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 4 transcripts, 1 regulatory feature and is associated with 3 phenotypes.

Variant displays