Variant #0000569806 (NC_000020.10:g.44519225dup, NM_001278535.1:c.406dup (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.44519225dup
DNA change (hg38) g.45890586dup
Published as CTSA(NM_000308.2):c.-740dup (p.(=)), NEURL2(NM_001278535.1):c.406dupA (p.S136Kfs*15)
ISCN -
DB-ID NEURL2_000001 See all 2 reported entries
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CTSA NM_000308.2 -?/. - c.-740dup r.(?) p.(=)
NEURL2 NM_001278535.1 -?/. - c.406dup r.(?) p.(Ser136LysfsTer15)
PLTP NM_006227.3 -?/. - c.*8355dup r.(?) p.(=)
SPATA25 NM_080608.3 -?/. - c.-2996dup r.(?) p.(=)


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