Variant #0000592769 (NC_000021.8:g.44492132G>A, NM_000071.2:c.172C>T (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.44492132G>A
DNA change (hg38) g.43072022G>A
Published as -
ISCN -
DB-ID CBS_000213 See all 4 reported entries
Variant remarks expression cloning in E.coli, CBs activity 0.013
Reference PubMed: de Franchis 1999
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
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 2020-07-16 22:29:58 +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 +/. 3 c.172C>T - r.(?) p.Arg58Trp


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