Variant #0000805825 (NC_000012.11:g.52681822A>T, NM_002284.3:c.-13879A>T (KRT86))

Chromosome 12
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.52681822A>T
DNA change (hg38) -
Published as KRT81(NM_002281.3):c.846T>A (p.Y282*), KRT81(NM_002281.4):c.846T>A (p.(Tyr282Ter))
ISCN -
DB-ID KRT81_000012 See all 2 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00112 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
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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.(Tyr282*)
KRT86 NM_002284.3 -?/. - c.-13879A>T r.(?) p.(=)


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