Variant #0000684730 (NC_000001.10:g.171076835A>G, FMO3(NM_001002294.2):c.341A>G)

Individual ID 00308683
Chromosome 1
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.171076835A>G
DNA change (hg38) g.171107694A>G
Published as -
ISCN -
DB-ID FMO3_000005 See all 3 reported entries
Variant remarks classification based on frequency in 305 unrelated individuals
Reference PubMed: Le 2019
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency frequency 0.014
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00074 View details
Owner Global Variome, with Curator vacancy
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
FMO3 NM_001002294.2 -?/. - c.341A>G - r.(?) p.(Asn114Ser)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000309828 DNA SEQ;SEQ-NG - 105 WGS/200 WES FMO3 1 Global Variome, with Curator vacancy