Variant #0000554537 (NC_000015.9:g.48704816G>A, NM_000138.4:c.8176C>T (FBN1))

Chromosome 15
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.48704816G>A
DNA change (hg38) g.48412619G>A
Published as FBN1(NM_000138.4):c.8176C>T (p.R2726W, p.(Arg2726Trp)), FBN1(NM_000138.5):c.8176C>T (p.R2726W)
ISCN -
DB-ID FBN1_000246 See all 6 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00072 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +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.8176C>T r.(?) p.(Arg2726Trp)


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