Variant #0000019551 (NC_000001.10:g.171076935C>T, NM_001002294.2:c.441C>T (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.171076935C>T |
| DNA change (hg38) |
g.171107794C>T |
| Published as |
15019A>C (S147S) |
| ISCN |
- |
| DB-ID |
FMO3_000092 See all 6 reported entries |
| Variant remarks |
- |
| Reference |
PubMed: Koukouritaki et al. 2005 |
| ClinVar ID |
- |
| dbSNP ID |
rs1800822 |
| Origin |
Germline |
| Segregation |
no |
| Frequency |
HapMap 0.066 (Eur), 0.227 (Jpn), 0.031 (Afr) |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.11445 View details |
| Owner |
Ian Phillips |
| Database submission license |
No license selected |
| Created by |
Ian Phillips |
| Date created |
2013-08-13 12:34:50 +02:00 (CEST) |
| Date last edited |
2017-04-05 10:58:51 +02:00 (CEST) |

Variant on transcripts
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