Variant #0000328450 (NC_000020.10:g.44520260_44520261del, NM_001278535.1:c.-631_-630del (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.44520260_44520261del
DNA change (hg38) g.45891621_45891622del
Published as CTSA(NM_000308.2):c.107_108del (p.(Leu36Profs*121))
ISCN -
DB-ID CTSA_000004
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2022-05-09 15:51:19 +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.107_108del r.(?) p.(Leu36ProfsTer121)
NEURL2 NM_001278535.1 -?/. - c.-631_-630del r.(?) p.(=)
PLTP NM_006227.3 -?/. - c.*7319_*7320del r.(=) p.(=)
SPATA25 NM_080608.3 -?/. - c.-4032_-4031del r.(?) p.(=)


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