Variant #0000000688 (NC_000015.9:g.48755393G>A, NM_000138.4:c.5110C>T (FBN1))

Chromosome 15
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.48755393G>A
Reference -
DB-ID FBN1_000011
Frequency -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Florian Bayersdorfer
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Florian Bayersdorfer
Date created 2025-10-06 08:23:13 +00:00 (UTC)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Class     
FBN1 NM_000138.4 +?/+? . c.5110C>T r.(?) p.(Gln1704*) likely pathogenic