Variant #0000435796 (NC_000022.10:g.51019870_51019878del, NM_005198.4:c.554_562del (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.51019870_51019878del
DNA change (hg38) g.50581441_50581449del
Published as -
ISCN -
DB-ID CHKB_000008 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 16:17:44 +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 +/. 4 c.554_562del r.(?) p.(Pro185_Trp187del)


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