Variant #0001041782 (NC_000017.10:g.3591400C>G, NM_001031681.2:c.*27372C>G (CTNS))

Chromosome 17
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.3591400C>G
DNA change (hg38) -
Published as P2RX5(NM_002561.4):c.888-1G>C
ISCN -
DB-ID CTNS_000083
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.*27372C>G r.(=) p.(=)
P2RX5 NM_002561.3 ?/. - c.888-1G>C r.spl? p.?
CTNS NM_004937.2 ?/. - c.*27737C>G r.(=) p.(=)
TAX1BP3 NM_014604.3 ?/. - c.-19580G>C r.(?) p.(=)
EMC6 NM_031298.2 ?/. - c.*18627C>G r.(=) p.(=)
P2RX5-TAX1BP3 NR_037928.1 ?/. - n.1287-1G>C r.(?) -


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