Variant #0000461385 (NC_000001.10:g.171077043_171077045del, FMO3(NM_001002294.2):c.484+65_484+67del)

Individual ID 00103177
Chromosome 1
Allele Parent #1
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.171077043_171077045del
DNA change (hg38) g.171107902_171107904del
Published as 20960_20962delCTT
ISCN -
DB-ID FMO3_000110
Variant remarks -
Reference PubMed: Fujieda 2003
ClinVar ID -
dbSNP ID -
Origin Germline
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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
FMO3 NM_001002294.2 -/. 4i c.484+65_484+67del - r.(=) p.(=)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000103631 DNA SEQ - - FMO3 5 Ornicha Prapapan