Variant #0000459067 (NC_000015.9:g.48936917A>G, NM_000138.4:c.50T>C (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.48936917A>G
DNA change (hg38) g.48644720A>G
Published as -
ISCN -
DB-ID FBN1_000219 See all 2 reported entries
Variant remarks classification based on FBN1-specific modified 2015 ACMGG/AMP/CAP criteria
Reference Baudhuin 2019, submitted
ClinVar ID -
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 No license selected
Created by Linnea Baudhuin
Date created 2019-02-21 18:29:31 +01:00 (CET)
Date last edited 2020-07-06 14:53:16 +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 ?/. - c.50T>C r.(?) p.Leu17Ser


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