Variant #0000459105 (NC_000015.9:g.48902966C>A, NM_000138.4:c.305G>T (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.48902966C>A
DNA change (hg38) g.48610769C>A
Published as -
ISCN -
DB-ID FBN1_000832 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 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2019-02-21 18:29:31 +01:00 (CET)
Date last edited 2020-07-06 14:53:03 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FBN1 NM_000138.4 +?/. 4 c.305G>T r.(?) p.Cys102Phe


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.