Variant #0001001371 (NC_000015.9:g.41797916del, NM_001135685.1:c.1302del (LTK))

Chromosome 15
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.41797916del
DNA change (hg38) -
Published as LTK(NM_002344.5):c.1692delC (p.(Ile565fs))
ISCN -
DB-ID ITPKA_000003
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) 1.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LTK NM_001135685.1 ?/. - c.1302del r.(?) p.(Ile435Serfs*28)
ITPKA NM_002220.2 ?/. - c.*2552del r.(?) p.(=)


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