Variant #0000530028 (NC_000007.13:g.100187407G>A, NC_000007.13(NM_001163499.1):c.3+141G>A (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.100187407G>A
DNA change (hg38) g.100589784G>A
Published as FBXO24(NM_012172.4):c.144G>A (p.E48=)
ISCN -
DB-ID FBXO24_000002
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) 0.00011 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.3+141G>A r.(=) p.(=)
LRCH4 NM_002319.3 -?/. - c.-3684C>T r.(?) p.(=)
PCOLCE-AS1 NR_038910.1 -?/. - n.2155C>T r.(?) -


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