Variant #0000850828 (NC_000005.9:g.147807365_147807370del, NC_000005.9(NM_030793.3):c.2428+80_2428+85del (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.147807365_147807370del
DNA change (hg38) -
Published as FBXO38(NM_205836.3):c.2508_2513delGAGTGG (p.S839_G840del)
ISCN -
DB-ID FBXO38_000026
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) Retrieve
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2022-05-09 15:40:45 +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     
FBXO38 NM_030793.3 -/. - c.2428+80_2428+85del r.(=) p.(=)
FBXO38 NM_030793.4 -/. - c.2428+80_2428+85del r.(=) p.(=)


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