Variant #0000605573 (NC_000001.10:g.240370684C>A, NM_020066.4:c.2572C>A (FMN2))
| Chromosome |
1 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
likely benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.240370684C>A |
| DNA change (hg38) |
g.240207384C>A |
| Published as |
FMN2(NM_001305424.1):c.2584C>A (p.P862T), FMN2(NM_020066.4):c.2572C>A (p.(Pro858Thr)) |
| ISCN |
- |
| DB-ID |
FMN2_000051 See all 2 reported entries |
| Variant remarks |
VKGL data sharing initiative Nederland |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
CLASSIFICATION record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.00108 View details |
| Owner |
VKGL-NL_Rotterdam |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Rotterdam |
| Date created |
2019-12-04 14:54:23 +01:00 (CET) |
| Date last edited |
2024-04-19 20:20:39 +02:00 (CEST) |

Variant on transcripts
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