Variant #0000802778 (NC_000007.13:g.100190594C>T, NM_001163499.1:c.711C>T (FBXO24))

Chromosome 7
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.100190594C>T
DNA change (hg38) -
Published as FBXO24(NM_033506.3):c.747C>T (p.I249=)
ISCN -
DB-ID FBXO24_000005
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) 2.0E-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 2021-09-17 14:40:49 +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     
FBXO24 NM_001163499.1 -?/. - c.711C>T r.(?) p.(Ile237=)
PCOLCE-AS1 NR_038910.1 -?/. - n.1608G>A r.(?) -


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