Variant #0001021747 (NC_000015.9:g.48936888C>T, NM_000138.4:c.79G>A (FBN1))

Chromosome 15
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method ACMG
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.48936888C>T
DNA change (hg38) g.48644691C>T
Published as -
ISCN -
DB-ID FBN1_000201 See all 5 reported entries
Variant remarks -
Reference PubMed: Drackley 2024, Journal: Drackley 2024
ClinVar ID ClinVar-163486
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00047 View details
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2025-01-28 16:37:02 +01:00 (CET)
Date last edited 2025-01-28 16:38:11 +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.79G>A r.(79G>A) p.(Ala27Thr)


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