Variant #0000167008 (NC_000001.10:g.171208224C>A, NM_002021.1:c.-69C>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.171208224C>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID FMO1_000009 See all 2 reported entries
Variant remarks associated with increased dose-adjusted serum OLA concentrations (C/Ds; P.0.008)
Variant Error [EREF/EREFSEQ]: This genomic variant does not match the reference sequence; the transcript variant also has an error. Please fix this entry and then remove this message.
Reference PubMed: Soderberg 2012
ClinVar ID -
dbSNP ID rs12720462
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Elizabeth A. Shephard
Database submission license No license selected
Created by Elizabeth A. Shephard
Date created 2013-08-07 10:16:37 +02:00 (CEST)
Date last edited N/A
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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 ?/? _1 c.-69C>A FMO1*6 r.(?) p.(=) -


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