Variant #0000167042 (NC_000001.10:g.171086481C>T, NM_001002294.2:c.1498C>T (FMO3))
| Chromosome |
1 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Affects function |
| Classification method |
- |
| Clinical classification |
NA |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.171086481C>T |
| DNA change (hg38) |
g.171117341C>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
FMO3_000016 See all 9 reported entries |
| Variant remarks |
abolishes activity for TMA and 5-DPT |
| Reference |
PubMed: Yamazaki 2007 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
2.0E-5 View details |
| Owner |
Ornicha Prapapan |
| Database submission license |
No license selected |
| Created by |
Ornicha Prapapan |
| Date created |
2013-05-15 15:35:52 +02:00 (CEST) |
| Date last edited |
2020-06-05 15:15:49 +02:00 (CEST) |

Variant on transcripts
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