Variant #0000616504 (NC_000017.10:g.38975328_38975339del, NM_000421.3:c.1448_1459del (KRT10))

Chromosome 17
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.38975328_38975339del
DNA change (hg38) g.40819076_40819087del
Published as KRT10(NM_000421.5):c.1448_1459delCCGGCGGCGGCC (p.S483_H487delinsY)
ISCN -
DB-ID KRT10_000057
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) 0.00093 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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KRT10 NM_000421.3 -?/. - c.1448_1459del r.(?) p.(Ser483_His487delinsTyr)
TMEM99 NM_145274.3 -?/. - c.-353_-342del r.(?) p.(=)


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