Variant #0001067565 (NC_000022.10:g.51018440T>G, NM_005198.4:c.890A>C (CHKB))

Chromosome 22
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.51018440T>G
DNA change (hg38) -
Published as CHKB(NM_005198.5):c.890A>C (p.(Lys297Thr))
ISCN -
DB-ID CHKB_000058
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2026-01-20 18:57:21 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CPT1B NM_001145134.1 ?/. - c.-1482A>C r.(?) p.(=)
CHKB NM_005198.4 ?/. - c.890A>C r.(?) p.(Lys297Thr)
CHKB-CPT1B NR_027928.2 ?/. - n.1108A>C r.(?) -


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