Variant #0000893484 (NC_000017.10:g.3558281C>T, NC_000017.10(NM_001031681.2):c.226-11C>T (CTNS))

Chromosome 17
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.3558281C>T
DNA change (hg38) -
Published as CTNS(NM_004937.3):c.226-11C>T
ISCN -
DB-ID CTNS_000069
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) 9.0E-5 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
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     
CTNS NM_001031681.2 -?/. - c.226-11C>T r.(=) p.(=)
CTNS NM_004937.2 -?/. - c.226-11C>T r.(=) p.(=)
TAX1BP3 NM_014604.3 -?/. - c.*8761G>A r.(=) p.(=)


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