Variant #0001021741 (NC_000015.9:g.48707733delinsAA, NM_000138.4:c.8051delinsTT (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.48707733delinsAA
DNA change (hg38) g.48415536delinsAA
Published as -
ISCN -
DB-ID FBN1_001565
Variant remarks -
Reference PubMed: Drackley 2024, Journal: Drackley 2024
ClinVar ID ClinVar-549451
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 InternationalCreative Commons License
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)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FBN1 NM_000138.4 +/. - c.8051delinsTT r.(8051delinsTT) p.(Gly2684ValfsTer21)


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