Variant #0001021737 (NC_000015.9:g.48713761_48713762delinsTTCACCTTCCAGATCACC, NM_000138.4:c.7692_7693delinsGGTGATCTGGAAGGTGAA (FBN1))
| Chromosome |
15 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
ACMG |
| Clinical classification |
likely pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.48713761_48713762delinsTTCACCTTCCAGATCACC |
| DNA change (hg38) |
g.48421564_48421565delinsTTCACCTTCCAGATCACC |
| Published as |
- |
| ISCN |
- |
| DB-ID |
FBN1_001566 |
| Variant remarks |
not yet formally curated |
| Reference |
PubMed: Drackley 2024, Journal: Drackley 2024 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2025-01-28 16:37:02 +01:00 (CET) |
| Date last edited |
2025-01-28 16:38:11 +01:00 (CET) |

Variant on transcripts
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