Original source

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

T/A/C|Ancestral: T|Ambiguity code: H

Chromosome 12:52677425 (forward strand)|View in location tab

Co-located variants

HGMD-PUBLIC CM981136, CM101644 ; PhenCode HIFD_KRT1:c.1019A>T (T/A), HIFD_KRT1:c.1019A>G (T/C)

Most severe consequence
Missense variant
Evidence status

Clinical significance


This variant has 3 synonyms - Show

HGVS names

This variant has 8 HGVS names - Show

About this variant

This variant overlaps 4 transcripts and is associated with 3 phenotypes.

Variant displays