Variant #0000019218 (NC_000001.10:g.171249965G>A, NM_002021.1:c.668G>A (FMO1))

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.171249965G>A
DNA change (hg38) g.171280826G>A
Published as g.22739G>A
ISCN -
DB-ID FMO1_000006
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs16864310
Origin Unknown
Segregation ?
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00018 View details
Owner Ornicha Prapapan
Database submission license No license selected
Created by Ornicha Prapapan
Date created 2013-07-28 12:34:01 +02:00 (CEST)
Date last edited 2016-08-05 16:42:31 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     

Enzyme activity     
FMO1 NM_002021.1 ?/? 6 c.668G>A - r.(?) p.(Arg223Gln) -


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