Variant #0000167105 (NC_000001.10:g.171076835A>G, FMO3(NM_001002294.2):c.341A>G)
Individual ID |
00103139 |
Chromosome |
1 |
Allele |
Maternal (confirmed) |
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.171076835A>G |
DNA change (hg38) |
g.171107694A>G |
Published as |
- |
ISCN |
- |
DB-ID |
FMO3_000005 See all 3 reported entries |
Variant remarks |
- |
Reference |
PubMed: Shimizu 2012 |
ClinVar ID |
- |
dbSNP ID |
rs186763441 |
Origin |
Germline |
Segregation |
no |
Frequency |
1/1280 chromosomes |
Re-site |
- |
VIP |
0 |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0.00074 View details |
Owner |
Ornicha Prapapan |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Johan den Dunnen |

Variant on transcripts
Screenings
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