Variant #0000167033 (NC_000001.10:g.171083242A>G, NM_001002294.2:c.923A>G (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 NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.171083242A>G
DNA change (hg38) g.171114102A>G
Published as -
ISCN -
DB-ID FMO3_000083 See all 12 reported entries
Variant remarks Sulindac: patients homozygous for E308G exhibit enhanced polyp regression in response to treatment
Reference PubMed: Sachse 1999, PubMed: Hisamuddin 2004, PubMed: Hisamuddin 2005, PubMed: Soderberg 2012
ClinVar ID -
dbSNP ID rs2266780
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.15101 View details
Owner Ornicha Prapapan
Database submission license No license selected
Created by Ornicha Prapapan
Date created 2013-02-17 17:53:25 +01:00 (CET)
Date last edited 2020-06-05 15:15:18 +02:00 (CEST)
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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.923A>G - r.(?) p.Glu308Gly


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