Variant #0001070245 (NC_000012.11:g.52681822A>T, NM_002281.3:c.846T>A (KRT81))

Chromosome 12
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.52681822A>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID KRT81_000012 See all 3 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs138597671
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00112 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2026-03-09 14:56:02 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KRT81 NM_002281.3 ?/. - c.846T>A r.(?) p.(Tyr282Ter)


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