Variant #0000856208 (NC_000022.10:g.51021173G>A, NM_005198.4:c.38C>T (CHKB))

Chromosome 22
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.51021173G>A
DNA change (hg38) -
Published as CHKB(NM_005198.4):c.38C>T (p.A13V)
ISCN -
DB-ID CHKB_000052
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) 0.00039 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:47:41 +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.-4215C>T r.(?) p.(=)
CHKB NM_005198.4 -?/. - c.38C>T r.(?) p.(Ala13Val)
CHKB-CPT1B NR_027928.2 -?/. - n.256C>T r.(?) -


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