Variant #0000019220 (NC_000001.10:g.171254485A>G, NM_002021.1:c.1401A>G (FMO1))
| Chromosome |
1 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Effect unknown |
| Classification method |
- |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.171254485A>G |
| DNA change (hg38) |
g.171285346A>G |
| Published as |
27258A>G |
| ISCN |
- |
| DB-ID |
FMO1_000008 |
| Variant remarks |
- |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
rs28360432 |
| Origin |
Germline |
| Segregation |
- |
| Frequency |
0.02 in Chinese |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.00261 View details |
| Owner |
Ornicha Prapapan |
| Database submission license |
No license selected |
| Created by |
Ornicha Prapapan |
| Date created |
2013-07-28 13:09:14 +02:00 (CEST) |
| Date last edited |
2017-04-04 22:34:36 +02:00 (CEST) |

Variant on transcripts
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