Variant #0001021738 (NC_000015.9:g.48936966T>G, NM_000138.4:c.1A>C (FBN1))
Chromosome |
15 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Classification method |
ACMG |
Clinical classification |
pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.48936966T>G |
DNA change (hg38) |
g.48644769T>G |
Published as |
- |
ISCN |
- |
DB-ID |
FBN1_001596 |
Variant remarks |
- |
Reference |
PubMed: Drackley 2024, Journal: Drackley 2024 |
ClinVar ID |
ClinVar-495569 |
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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