Variant #0000879678 (NC_000011.9:g.63974966G>A, NM_031471.5:c.130G>A (FERMT3))
| Chromosome |
11 |
| 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.63974966G>A |
| DNA change (hg38) |
g.64207494G>A |
| Published as |
- |
| ISCN |
- |
| DB-ID |
FERMT3_000013 See all 3 reported entries |
| Variant remarks |
- |
| Reference |
PubMed: Roos 2023, Journal: Roos 2023 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.00595 View details |
| Owner |
Dirk Roos |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2022-09-27 17:12:21 +02:00 (CEST) |
| Date last edited |
2025-01-23 20:45:08 +01:00 (CET) |

Variant on transcripts
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