Variant #0000524745 (NC_000005.9:g.147813013G>A, NM_030793.3:c.2455G>A (FBXO38))

Chromosome 5
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.147813013G>A
DNA change (hg38) g.148433450G>A
Published as FBXO38(NM_030793.5):c.2455G>A (p.A819T)
ISCN -
DB-ID FBXO38_000015
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) 0.00774 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2022-05-09 15:24:52 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FBXO38 NM_030793.3 -/. - c.2455G>A r.(?) p.(Ala819Thr)
FBXO38 NM_030793.4 -/. - c.2455G>A r.(?) p.(Ala819Thr)


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