Variant #0000727704 (NC_000020.10:g.44523674dup, NM_001278535.1:c.-4038dup (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.44523674dup
DNA change (hg38) -
Published as CTSA(NM_001127695.2):c.990dupC (p.C331Lfs*56)
ISCN -
DB-ID CTSA_000039
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-02-08 18:36:18 +01:00 (CET)
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.1044dup r.(?) p.(Cys349Leufs*56)
NEURL2 NM_001278535.1 ?/. - c.-4038dup r.(?) p.(=)
PLTP NM_006227.3 ?/. - c.*3912dup r.(?) p.(=)


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