Variant #0000809683 (NC_000022.10:g.51018650_51018652del, NM_005198.4:c.788_790del (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.51018650_51018652del
DNA change (hg38) -
Published as CHKB(NM_005198.5):c.788_790delTGG (p.V263del)
ISCN -
DB-ID CHKB_000047
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2021-09-17 14:40:49 +02:00 (CEST)
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.-1691_-1689del r.(?) p.(=)
CHKB NM_005198.4 ?/. - c.788_790del r.(?) p.(Val263del)
CHKB-CPT1B NR_027928.2 ?/. - n.1006_1008del r.(?) -


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