Variant #0000569814 (NC_000020.10:g.44520892G>A, NM_001278535.1:c.-1262C>T (NEURL2))

Chromosome 20
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.44520892G>A
DNA change (hg38) g.45892253G>A
Published as CTSA(NM_000308.2):c.361-20G>A (p.(=))
ISCN -
DB-ID CTSA_000021
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) 1.0E-5 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)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CTSA NM_000308.2 ?/. - c.361-20G>A r.(=) p.(=)
NEURL2 NM_001278535.1 ?/. - c.-1262C>T r.(?) p.(=)
PLTP NM_006227.3 ?/. - c.*6688C>T r.(=) p.(=)
SPATA25 NM_080608.3 ?/. - c.-4663C>T r.(?) p.(=)


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