Variant #0000914789 (NC_000017.10:g.3552198_3552218del, NM_001031681.2:c.198_218del (CTNS))

Chromosome 17
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.3552198_3552218del
DNA change (hg38) -
Published as -
ISCN -
DB-ID CTNS_000004 See all 6 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) 2.0E-5 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2023-01-11 15:44:22 +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.198_218del r.(?) p.(Ile67_Pro73del)
CTNS NM_004937.2 +?/. - c.198_218del r.(?) p.(Ile67_Pro73del)
TAX1BP3 NM_014604.3 +?/. - c.*14824_*14844del r.(=) p.(=)


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