Variant #0000689454 (NC_000005.9:g.147774350G>A, NM_030793.3:c.11G>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.147774350G>A
DNA change (hg38) -
Published as FBXO38(NM_205836.2):c.11G>A (p.R4Q)
ISCN -
DB-ID FBXO38_000020
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) 8.0E-5 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 2020-09-15 15:50:26 +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.11G>A r.(?) p.(Arg4Gln)
FBXO38 NM_030793.4 ?/. - c.11G>A r.(?) p.(Arg4Gln)


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