Variant #0000021376 (NC_000001.10:g.171076966G>A, FMO3(NM_001002294.2):c.472G>A)

Individual ID 00103150
Chromosome 1
Allele Both (homozygous)
Affects function (as reported) Probably affects function
Affects function (by curator) Effect unknown
Classification method -
Clinical classification likely pathogenic (recessive)
DNA change (genomic) (Relative to hg19 / GRCh37) g.171076966G>A
DNA change (hg38) g.171107825G>A
Published as -
ISCN -
DB-ID FMO3_000008 See all 27 reported entries
Variant remarks -
Reference PubMed: Ferreira 2013
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) 0.37494 View details
Owner Elizabeth A. Shephard
Database submission license No license selected
Created by Elizabeth A. Shephard
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
FMO3 NM_001002294.2 +?/? 4 c.472G>A - r.(?) p.(Glu158Lys)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000103604 DNA SEQ - - FMO3 2 Elizabeth A. Shephard