Variant #0001027344 (NC_000021.8:g.45194178G>A, NM_000100.3:c.202C>T (CSTB))

Chromosome 21
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.45194178G>A
DNA change (hg38) -
Published as CSTB(NM_000100.3):c.202C>T (p.R68*), CSTB(NM_000100.4):c.202C>T (p.R68*)
ISCN -
DB-ID CSTB_000005 See all 7 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) 4.0E-5 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2025-02-07 18:57:27 +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     
CSTB NM_000100.3 +/. - c.202C>T r.(?) p.(Arg68Ter)


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