Variant #0000592768 (NC_000021.8:g.[44488629C>G;44488702G>C], NM_000071.2:c.[233C>G;306G>C] (CBS))

Chromosome 21
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.[44488629C>G;44488702G>C]
DNA change (hg38) g.[43068519C>G;43068592G>C]
Published as -
ISCN -
DB-ID CBS_000058
Variant remarks expression cloning in E.coli, CBs activity 0
Reference PubMed: de Franchis 1994
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2019-08-16 14:04:43 +02:00 (CEST)
Date last edited 2019-08-16 14:06:09 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
CBS NM_000071.2 +/. 4 c.[233C>G;306G>C] - - p.[Pro78Arg;Lys12Asn]


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