Genomic variant #0000018020

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 0
Methylation -
Average frequency (large NGS studies) Variant not found in online data sets
Owner Ornicha Prapapan
Options




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