Variant #0000017176 (NC_000001.10:g.171083403G>C, FMO3(NM_001002294.2):c.1084G>C)

Individual ID 00103186
Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.171083403G>C
DNA change (hg38) g.171114263G>C
Published as g.21604G>C
ISCN -
DB-ID FMO3_000039 See all 2 reported entries
Variant remarks 2/100 chromosomes (African American); db SNP: 1/126 chromosomes (African), 0/130 chromosomes (European), 0/88 chromosomes (Asian)
Reference PubMed: Cashman et al. 2002, PubMed: Furnes et al. 2003,
ClinVar ID -
dbSNP ID rs2066532
Origin Germline
Segregation no
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00095 View details
Owner Ornicha Prapapan
Database submission license No license selected
Created by Ornicha Prapapan
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
FMO3 NM_001002294.2 ?/? 7 c.1084G>C - r.(?) p.(Glu362Gln)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000103640 DNA SEQ - - FMO3 1 Ornicha Prapapan