Variant #0000001486 (NC_000021.8:g.45194568C>G, NM_000100.3:c.139G>C (CSTB))

Chromosome 21
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.45194568C>G
DNA change (hg38) g.43774687C>G
Published as -
ISCN -
DB-ID CSTB_000016
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs140799752
Origin SUMMARY record
Segregation -
Frequency 0.000 1000Gen
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 2012-08-27 11:26:13 +02:00 (CEST)
Date last edited 2022-03-10 09:55:26 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CSTB NM_000100.3 ?/. 2 c.139G>C r.(139g>c) p.(Val47Leu)


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