Variant #0000459672 (NC_000015.9:g.48714179C>T, NM_000138.4:c.7540G>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.48714179C>T |
DNA change (hg38) |
g.48421982C>T |
Published as |
- |
ISCN |
- |
DB-ID |
FBN1_000299 See all 3 reported entries |
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 14:47:10 +02:00 (CEST) |

Variant on transcripts
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