Variant #0001021737 (NC_000015.9:g.48713761_48713762delinsTTCACCTTCCAGATCACC, NM_000138.4:c.7692_7693delinsGGTGATCTGGAAGGTGAA (FBN1))

Chromosome 15
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method ACMG
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.48713761_48713762delinsTTCACCTTCCAGATCACC
DNA change (hg38) g.48421564_48421565delinsTTCACCTTCCAGATCACC
Published as -
ISCN -
DB-ID FBN1_001566
Variant remarks not yet formally curated
Reference PubMed: Drackley 2024, Journal: Drackley 2024
ClinVar ID -
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.7692_7693delinsGGTGATCTGGAAGGTGAA r.(7692_7693delinsGGTGATCTGGAAGGTGAA) p.(Ser2564ArgfsTer8)


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