Variant #0000001455 (NC_000021.8:g.45194641C>G, NC_000021.8(NM_000100.3):c.67-1G>C (CSTB))

Chromosome 21
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic (recessive)
DNA change (genomic) (Relative to hg19 / GRCh37) g.45194641C>G
DNA change (hg38) g.43774760C>G
Published as -
ISCN -
DB-ID CSTB_000001 See all 16 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs147484110
Origin SUMMARY record
Segregation -
Frequency 2/6503 NHLBI
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00015 View details
Owner Anne Polvi
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Anne Polvi
Date created 2012-08-06 10:16:36 +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 +/. 1i c.67-1G>C r.spl? p.?


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