Variant #0000616503 (NC_000017.10:g.38975327_38975328insAGCCGCCGCC, NM_000421.3:c.1459_1460insGGCGGCGGCT (KRT10))

Chromosome 17
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.38975327_38975328insAGCCGCCGCC
DNA change (hg38) g.40819075_40819076insAGCCGCCGCC
Published as KRT10(NM_000421.3):c.1459_1460insGGCGGCGGCT (p.H487Rfs*97), KRT10(NM_000421.5):c.1459_1460insGGCGGCGGCT (p.(His487Argfs*97)), KRT10(NM_000421.5):c....
ISCN -
DB-ID KRT10_000056 See all 3 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) 0.00221 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 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     
KRT10 NM_000421.3 ?/. - c.1459_1460insGGCGGCGGCT r.(?) p.(His487ArgfsTer97)
TMEM99 NM_145274.3 ?/. - c.-354_-353insAGCCGCCGCC r.(?) p.(=)


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