Variant #0000459089 (NC_000015.9:g.48936814G>T, NM_000138.4:c.153C>A (FBN1))
| Chromosome |
15 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Not classified |
| Classification method |
ACMG |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.48936814G>T |
| DNA change (hg38) |
g.48644617G>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
FBN1_000848 |
| Variant remarks |
classification based on FBN1-specific modified 2015 ACMGG/AMP/CAP criteria |
| Reference |
Baudhuin 2019, submitted |
| ClinVar ID |
present |
| dbSNP ID |
- |
| Origin |
CLASSIFICATION record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Linnea Baudhuin |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2019-02-21 18:29:31 +01:00 (CET) |
| Date last edited |
2020-07-06 14:53:12 +02:00 (CEST) |

Variant on transcripts
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