Variant #0000000295 (NC_000015.9:g.48808549G>C, NM_000138.4:c.1158C>G (FBN1))

Chromosome 15
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
DNA change (genomic) (Relative to hg19 / GRCh37) g.48808549G>C
Reference -
DB-ID FBN1_000005
Frequency -
Average frequency (gnomAD v.2.1.1) 7.0E-5 View details
Owner Florian Bayersdorfer
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Florian Bayersdorfer
Date created 2023-06-29 13:24:45 +00:00 (UTC)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FBN1 NM_000138.4 ?/? 11 c.1158C>G r.(?) p.(Asn386Lys)