Variant #0000569816 (NC_000020.10:g.44521137C>T, NM_001278535.1:c.-1507G>A (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.44521137C>T
DNA change (hg38) g.45892498C>T
Published as CTSA(NM_000308.2):c.498+14C>T (p.(=))
ISCN -
DB-ID CTSA_000023
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) 0.00346 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2022-05-09 15:51:19 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CTSA NM_000308.2 -?/. - c.498+14C>T r.(=) p.(=)
NEURL2 NM_001278535.1 -?/. - c.-1507G>A r.(?) p.(=)
PLTP NM_006227.3 -?/. - c.*6443G>A r.(=) p.(=)
SPATA25 NM_080608.3 -?/. - c.-4908G>A r.(?) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.