Variant #0001043365 (NC_000020.10:g.44519922G>T, NM_001278535.1:c.-292C>A (NEURL2))

Chromosome 20
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.44519922G>T
DNA change (hg38) -
Published as CTSA(NM_000308.2):c.-43G>T (p.(=))
ISCN -
DB-ID CTSA_000063
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) 0.02779 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 2025-05-05 21:14:00 +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     
CTSA NM_000308.2 -?/. - c.-43G>T r.(?) p.(=)
NEURL2 NM_001278535.1 -?/. - c.-292C>A r.(?) p.(=)
PLTP NM_006227.3 -?/. - c.*7658C>A r.(=) p.(=)
SPATA25 NM_080608.3 -?/. - c.-3693C>A r.(?) p.(=)


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