Variant #0000592785 (NC_000021.8:g.44483098C>T, NM_000071.2:c.919G>A (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.44483098C>T
DNA change (hg38) g.43062988C>T
Published as -
ISCN -
DB-ID CBS_000122 See all 79 reported entries
Variant remarks expression cloning in E.coli, CBs activity 0
Reference PubMed: Hu 1993
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00015 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 22:28:19 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
CBS NM_000071.2 +/. 10 c.919G>A - r.(?) p.Gly37Ser


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.