Variant #0000968822 (NC_000017.10:g.3561334C>T, NM_001031681.2:c.717C>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.3561334C>T
DNA change (hg38) -
Published as CTNS(NM_004937.3):c.717C>T (p.G239=)
ISCN -
DB-ID CTNS_000075
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2024-02-26 20:06:56 +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.717C>T r.(?) p.(=)
P2RX5 NM_002561.3 -?/. - c.*15828G>A r.(=) p.(=)
CTNS NM_004937.2 -?/. - c.717C>T r.(?) p.(=)
TAX1BP3 NM_014604.3 -?/. - c.*5708G>A r.(=) p.(=)
EMC6 NM_031298.2 -?/. - c.-10909C>T r.(?) p.(=)


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