Variant #0000895345 (NC_000020.10:g.44523553G>T, NM_001278535.1:c.-3923C>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.44523553G>T
DNA change (hg38) -
Published as CTSA(NM_000308.2):c.1002+13G>T (p.(=))
ISCN -
DB-ID CTSA_000049
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) 0.00021 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 2022-11-01 13:41:49 +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.1002+13G>T r.(=) p.(=)
NEURL2 NM_001278535.1 -?/. - c.-3923C>A r.(?) p.(=)
PLTP NM_006227.3 -?/. - c.*4027C>A r.(=) p.(=)


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