Variant #0000895822 (NC_000022.10:g.51020208del, NM_005198.4:c.419del (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.51020208del
DNA change (hg38) -
Published as CHKB(NM_005198.4):c.419delC (p.P140Qfs*14)
ISCN -
DB-ID CHKB_000048 See all 2 reported entries
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 2022-11-01 13:41:49 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CPT1B NM_001145134.1 +/. - c.-3248del r.(?) p.(=)
CHKB NM_005198.4 +/. - c.419del r.(?) p.(Pro140Glnfs*14)
CHKB-CPT1B NR_027928.2 +/. - n.637del r.(?) -


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