Genomic variant #0000461355

Individual ID 00226200
Chromosome 1
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Does not affect function
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.171080080G>A
DNA change (hg38) g.171110939G>A
Published as Val257Met
ISCN -
DB-ID FMO3_000009 See all 6 reported entries
Variant remarks not in 200 control chromosomes
Reference PubMed: Ferreira 2013
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (large NGS studies) 0.05843 View details
Owner Johan den Dunnen
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
FMO3 NM_001002294.2 +?/- 6 c.769G>A - r.(?) p.(Val257Met)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000227275 DNA SEQ - - FMO3 2 Johan den Dunnen