Variant #0000548532 (NC_000012.11:g.52681056C>T, NM_002284.3:c.-14645C>T (KRT86))

Chromosome 12
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.52681056C>T
DNA change (hg38) g.52287272C>T
Published as KRT81(NM_002281.4):c.1077G>A (p.A359=)
ISCN -
DB-ID KRT81_000003 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) 0.3475 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-12-07 15:54:56 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KRT81 NM_002281.3 -/. - c.1077G>A r.(?) p.(Ala359=)
KRT86 NM_002284.3 -/. - c.-14645C>T r.(?) p.(=)


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