Variant #0000459089 (NC_000015.9:g.48936814G>T, NM_000138.4:c.153C>A (FBN1))

Chromosome 15
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method ACMG
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.48936814G>T
DNA change (hg38) g.48644617G>T
Published as -
ISCN -
DB-ID FBN1_000848
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 14:53:12 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FBN1 NM_000138.4 ?/. 2 c.153C>A r.(?) p.Asp51Glu


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