Variant #0000167124 (NC_000001.10:g.171086382_171086579del, FMO3(NM_001002294.2):c.(1399_1596del))

Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.171086382_171086579del
DNA change (hg38) g.171117242_171117439del
Published as -
ISCN -
DB-ID FMO3_000000 See all 4 reported entries
Variant remarks cDNA expression cloning in E.coli shows no N-oxygenation activity
Reference PubMed: Yamazaki 2007
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
FMO3 NM_001002294.2 +/+ 9 c.(1399_1596del) - r.(?) p.Ser467*