Variant #0000287341 (NC_000022.10:g.32875190G>A, NM_001033024.1:c.108G>A (FBXO7))
| Chromosome |
22 |
| Allele |
Unknown |
| Affects function (as reported) |
Does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.32875190G>A |
| DNA change (hg38) |
g.32479203G>A |
| Published as |
FBXO7(NM_001257990.2):c.3G>A (p.M1?), FBXO7(NM_012179.3):c.345G>A (p.M115I), FBXO7(NM_012179.4):c.345G>A (p.M115I) |
| ISCN |
- |
| DB-ID |
FBXO7_000006 See all 3 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) |
0.4527 View details |
| Owner |
VKGL-NL_Rotterdam |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Rotterdam |
| Date created |
2018-01-15 20:58:59 +01:00 (CET) |
| Date last edited |
2023-01-11 15:44:22 +01:00 (CET) |

Variant on transcripts
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