Variant #0000253158 (NC_000022.10:g.32880006A>G, NM_001033024.1:c.303A>G (FBXO7))

Chromosome 22
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.32880006A>G
DNA change (hg38) g.32484019A>G
Published as FBXO7(NM_012179.3):c.540A>G (p.P180=), FBXO7(NM_012179.4):c.540A>G (p.P180=)
ISCN -
DB-ID FBXO7_000007 See all 4 reported entries
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) 0.03429 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FBXO7 NM_001033024.1 -/. - c.303A>G r.(?) p.(Pro101=)


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