Variant #0000276683 (NC_000005.9:g.147819364C>T, NC_000005.9(NM_030793.3):c.2945+9C>T (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.147819364C>T
DNA change (hg38) g.148439801C>T
Published as FBXO38(NM_030793.5):c.2945+9C>T
ISCN -
DB-ID FBXO38_000009
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 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.2945+9C>T r.(=) p.(=)
FBXO38 NM_030793.4 -/. - c.2945+9C>T r.(=) p.(=)


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