Variant #0000982445 (NC_000017.10:g.3563556C>A, NM_001031681.2:c.997C>A (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.3563556C>A
DNA change (hg38) -
Published as CTNS(NM_004937.3):c.997C>A (p.(Pro333Thr))
ISCN -
DB-ID CTNS_000078
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 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CTNS NM_001031681.2 ?/. - c.997C>A r.(?) p.(Pro333Thr)
P2RX5 NM_002561.3 ?/. - c.*13606G>T r.(=) p.(=)
CTNS NM_004937.2 ?/. - c.997C>A r.(?) p.(Pro333Thr)
TAX1BP3 NM_014604.3 ?/. - c.*3486G>T r.(=) p.(=)
EMC6 NM_031298.2 ?/. - c.-8687C>A r.(?) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.