Variant #0001041779 (NC_000017.10:g.3560089G>A, NM_001031681.2:c.681G>A (CTNS))

Chromosome 17
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.3560089G>A
DNA change (hg38) -
Published as CTNS(NM_004937.3):c.681G>A (p.(Glu227=))
ISCN -
DB-ID CTNS_000056 See all 2 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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CTNS NM_001031681.2 +/. - c.681G>A r.(?) p.(Glu227=)
CTNS NM_004937.2 +/. - c.681G>A r.(?) p.(Glu227=)
TAX1BP3 NM_014604.3 +/. - c.*6953C>T r.(=) p.(=)


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