Variant #0000569812 (NC_000020.10:g.44520261_44520263dup, NM_001278535.1:c.-610_-608dup (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.44520261_44520263dup
DNA change (hg38) g.45891622_45891624dup
Published as CTSA(NM_000308.2):c.108_110dup (p.(Leu37dup)), CTSA(NM_001127695.2):c.54_56dupGCT (p.L19dup), CTSA(NM_001127695.3):c.54_56dupGCT (p.L19dup)
ISCN -
DB-ID CTSA_000020 See all 3 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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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.108_110dup r.(?) p.(Leu37dup)
NEURL2 NM_001278535.1 -?/. - c.-610_-608dup r.(?) p.(=)
PLTP NM_006227.3 -?/. - c.*7340_*7342dup r.(=) p.(=)
SPATA25 NM_080608.3 -?/. - c.-4011_-4009dup r.(?) p.(=)


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