Variant #0000984320 (NC_000022.10:g.51009960C>T, NM_001145134.1:c.1482G>A (CPT1B))

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.51009960C>T
DNA change (hg38) -
Published as CPT1B(NM_152246.3):c.1584G>A (p.(Ala528=))
ISCN -
DB-ID CHKB-CPT1B_000004
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) 0.00019 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
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.1482G>A r.(?) p.(=)
CHKB-CPT1B NR_027928.2 ?/. - n.3154G>A r.(?) -


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