Variant #0001001372 (NC_000015.9:g.41800377T>C, NM_001135685.1:c.956A>G (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.41800377T>C
DNA change (hg38) -
Published as LTK(NM_002344.5):c.1139A>G (p.(Asn380Ser))
ISCN -
DB-ID ITPKA_000004
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) 8.0E-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.956A>G r.(?) p.(Asn319Ser)
ITPKA NM_002220.2 ?/. - c.*5013T>C r.(=) p.(=)


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