Variant #0000530029 (NC_000007.13:g.100187951G>A, NM_001163499.1:c.257G>A (FBXO24))

Chromosome 7
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.100187951G>A
DNA change (hg38) g.100590328G>A
Published as FBXO24(NM_033506.3):c.293G>A (p.R98Q)
ISCN -
DB-ID FBXO24_000003
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) 4.0E-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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FBXO24 NM_001163499.1 ?/. - c.257G>A r.(?) p.(Arg86Gln)
LRCH4 NM_002319.3 ?/. - c.-4228C>T r.(?) p.(=)
PCOLCE-AS1 NR_038910.1 ?/. - n.1758C>T r.(?) -


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