Variant #0000276680 (NC_000005.9:g.147805120T>C, NM_030793.3:c.1774T>C (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.147805120T>C
DNA change (hg38) g.148425557T>C
Published as FBXO38(NM_030793.5):c.1774T>C (p.S592P)
ISCN -
DB-ID FBXO38_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) 0.26813 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.1774T>C r.(?) p.(Ser592Pro)
FBXO38 NM_030793.4 -/. - c.1774T>C r.(?) p.(Ser592Pro)


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