Variant #0000728231 (NC_000022.10:g.51019955G>A, NM_005198.4:c.475C>T (CHKB))

Chromosome 22
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.51019955G>A
DNA change (hg38) -
Published as CHKB(NM_005198.5):c.475C>T (p.R159*)
ISCN -
DB-ID CHKB_000035
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CPT1B NM_001145134.1 +?/. - c.-2997C>T r.(?) p.(=)
CHKB NM_005198.4 +?/. - c.475C>T r.(?) p.(Arg159Ter)
CHKB-CPT1B NR_027928.2 +?/. - n.693C>T r.(?) -


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