Variant #0001005417 (NC_000020.10:g.44520261del, NM_001278535.1:c.-631del (NEURL2))

Chromosome 20
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.44520261del
DNA change (hg38) -
Published as CTSA(NM_000308.2):c.108delG (p.(Leu37fs))
ISCN -
DB-ID CTSA_000059
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) Retrieve
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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CTSA NM_000308.2 ?/. - c.108del r.(?) p.(Leu37*)
NEURL2 NM_001278535.1 ?/. - c.-631del r.(?) p.(=)
PLTP NM_006227.3 ?/. - c.*7319del r.(?) p.(=)
SPATA25 NM_080608.3 ?/. - c.-4032del r.(?) p.(=)


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