Variant #0000915382 (NC_000020.10:g.44520261_44520263del, NM_001278535.1:c.-610_-608del (NEURL2))

Chromosome 20
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.44520261_44520263del
DNA change (hg38) -
Published as CTSA(NM_000308.2):c.85_87del (p.(Leu37del)), CTSA(NM_001127695.2):c.54_56delGCT (p.L19del), CTSA(NM_001127695.3):c.54_56delGCT (p.L19del)
ISCN -
DB-ID CTSA_000002 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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2023-01-11 15:44:22 +01:00 (CET)
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.108_110del r.(?) p.(Leu37del)
NEURL2 NM_001278535.1 -/. - c.-610_-608del r.(?) p.(=)
PLTP NM_006227.3 -/. - c.*7340_*7342del r.(=) p.(=)
SPATA25 NM_080608.3 -/. - c.-4011_-4009del r.(?) p.(=)


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