Variant #0000276684 (NC_000005.9:g.147821690G>A, NM_030793.3:c.3322G>A (FBXO38))

Chromosome 5
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.147821690G>A
DNA change (hg38) g.148442127G>A
Published as FBXO38(NM_030793.5):c.3322G>A (p.V1108I)
ISCN -
DB-ID FBXO38_000011
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) 0.00064 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 2018-01-15 20:58:59 +01:00 (CET)
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.3322G>A r.(?) p.(Val1108Ile)
FBXO38 NM_030793.4 ?/. - c.3322G>A r.(?) p.(Val1108Ile)


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