Variant #0000572408 (NC_000022.10:g.51018620del, NM_005198.4:c.817del (CHKB))

Chromosome 22
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.51018620del
DNA change (hg38) g.50580191del
Published as -
ISCN -
DB-ID CHKB_000033
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CPT1B NM_001145134.1 +/. - c.-1662del r.(?) p.(=)
CHKB NM_005198.4 +/. - c.817del r.(?) p.(Arg273GlyfsTer68)
CHKB-CPT1B NR_027928.2 +/. - n.1035del r.(?) -


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