Variant #0000167054 (NC_000001.10:g.171083242A>G, NM_001002294.2:c.923A>G (FMO3))

Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
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 little/moderate substrate-dependent effec, results vary among lab, effect greater when present in cis with p.Glu158Lys: Kcat/Km for methimazole reduced 18% (p.Glu308Gly) and 57% (p.Glu158Lys-Glu308Gly) (Allerston 2009).
Reference PubMed: Zschocke 1999
ClinVar ID -
dbSNP ID rs3832024
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 2013-03-11 23:06:16 +01:00 (CET)
Date last edited 2020-06-05 15:15:19 +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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