Variant #0000001427 (NC_000021.8:g.45196141C>G, NM_000100.3:c.10G>C (CSTB))

Chromosome 21
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic (recessive)
DNA change (genomic) (Relative to hg19 / GRCh37) g.45196141C>G
DNA change (hg38) g.43776260C>G
Published as -
ISCN -
DB-ID CSTB_000003 See all 3 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs74315443
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Anne Polvi
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Anne Polvi
Date created 2012-08-01 13:42:59 +02:00 (CEST)
Date last edited 2022-03-10 09:54:15 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CSTB NM_000100.3 +?/. 1 c.10G>C r.(10g>c) p.(Gly4Arg)


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