Variant #0000435795 (NC_000022.10:g.51017668C>A, NM_005198.4:c.1130G>T (CHKB))

Chromosome 22
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.51017668C>A
DNA change (hg38) g.50579239C>A
Published as -
ISCN -
DB-ID CHKB_000007 See all 3 reported entries
Variant remarks cloned, purified enzyme activity <30%
Reference PubMed: Mitsuhashi 2011
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 2011-06-28 16:30:12 +02:00 (CEST)
Date last edited 2020-07-17 16:16:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CHKB NM_005198.4 +/. 11 c.1130G>T r.(?) p.(Arg377Leu)


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