Variant #0000017090 (NC_000001.10:g.171076835A>G, NM_001002294.2:c.341A>G (FMO3))
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.171076835A>G |
DNA change (hg38) |
g.171107694A>G |
Published as |
g.15036A>G |
ISCN |
- |
DB-ID |
FMO3_000005 See all 3 reported entries |
Variant remarks |
not causative of TMAU, no effect in vitro |
Reference |
PubMed: Shimizu et al. 2007 |
ClinVar ID |
- |
dbSNP ID |
rs186763441 |
Origin |
Germline |
Segregation |
no |
Frequency |
0/100 chromosomes |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0.00074 View details |
Owner |
Ornicha Prapapan |
Database submission license |
No license selected |
Created by |
Ornicha Prapapan |
Date created |
2013-02-19 22:30:03 +01:00 (CET) |
Date last edited |
2017-04-05 15:03:22 +02:00 (CEST) |

Variant on transcripts
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