Variant #0000019218 (NC_000001.10:g.171249965G>A, NM_002021.1:c.668G>A (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.171249965G>A |
| DNA change (hg38) |
g.171280826G>A |
| Published as |
g.22739G>A |
| ISCN |
- |
| DB-ID |
FMO1_000006 |
| Variant remarks |
- |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
rs16864310 |
| Origin |
Unknown |
| Segregation |
? |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.00018 View details |
| Owner |
Ornicha Prapapan |
| Database submission license |
No license selected |
| Created by |
Ornicha Prapapan |
| Date created |
2013-07-28 12:34:01 +02:00 (CEST) |
| Date last edited |
2016-08-05 16:42:31 +02:00 (CEST) |

Variant on transcripts
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