Variant #0000167058 (NC_000001.10:g.171077274G>T, NM_001002294.2:c.539G>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 NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.171077274G>T
DNA change (hg38) g.171108133G>T
Published as -
ISCN -
DB-ID FMO3_000042 See all 4 reported entries
Variant remarks no effect on N-oxygenation of TMA or S-oxygenation of methimazole
Reference PubMed: Dolphin 2000
ClinVar ID -
dbSNP ID rs75904274
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.01258 View details
Owner Ornicha Prapapan
Database submission license No license selected
Created by Ornicha Prapapan
Date created 2013-03-21 14:57:25 +01:00 (CET)
Date last edited 2020-06-05 15:14:49 +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 -/- 5 c.539G>T - r.(?) p.Gly180Val


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