Variant #0000459085 (NC_000015.9:g.48936843C>G, NM_000138.4:c.124G>C (FBN1))

Chromosome 15
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method ACMG
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.48936843C>G
DNA change (hg38) g.48644646C>G
Published as -
ISCN -
DB-ID FBN1_000852
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) 3.0E-5 View details
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 14:53:13 +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.124G>C r.(?) p.Ala42Pro


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