Variant #0000019555 (NC_000001.10:g.171059211C>T, NM_001002294.2:c.-918C>T (FMO3))

Chromosome 1
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Does not affect function
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.171059211C>T
DNA change (hg38) g.171090070C>T
Published as -2589C>T
ISCN -
DB-ID FMO3_000096
Variant remarks no effect on transcription in vitro
Reference PubMed: Koukouritaki et al. 2005
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation ?
Frequency 0.040 (white American), 0.007 (African American), 0.007 (Hispanic American)
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Ian Phillips
Database submission license No license selected
Created by Ian Phillips
Date created 2013-08-14 15:46:48 +02:00 (CEST)
Date last edited 2017-04-05 11:00:42 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
FMO3 NM_001002294.2 -/- _1 c.-918C>T - r.(=) p.(=)


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