Variant #0000018020 (NC_000001.10:g.171072929C>A, NM_001002294.2:c.136C>A (FMO3))

Individual ID 00103143
Chromosome 1
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Does not affect function
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.171072929C>A
DNA change (hg38) g.171103788C>A
Published as -
ISCN -
DB-ID FMO3_000046
Variant remarks Rare variant. 1/140 chromosomes in Koreans
Reference PubMed: Park et al. 1999
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation no
Frequency 1/140 chromosomes
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Ornicha Prapapan
Database submission license No license selected
Created by Ornicha Prapapan
Date created 2013-05-13 14:08:46 +02:00 (CEST)
Date last edited 2017-04-05 10:54:58 +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 -/- 3 c.136C>A - r.(?) p.(His46Asn)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000103597 DNA SEQ - - FMO3 1 Ornicha Prapapan


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