Variant #0000461384 (NC_000001.10:g.171076935C>T, FMO3(NM_001002294.2):c.441C>T)

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.171076935C>T
DNA change (hg38) g.171107794C>T
Published as 20852C>T
ISCN -
DB-ID FMO3_000092 See all 6 reported entries
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) 0.11445 View details
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 -/. - c.441C>T - r.(=) p.(=)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000103631 DNA SEQ - - FMO3 5 Ornicha Prapapan