Variant #0001007078 (NC_000015.9:g.48936960G>A, NM_000138.4:c.7C>T (FBN1))

Chromosome 15
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.48936960G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID FBN1_001545
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs886038797
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2024-09-04 14:09:02 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FBN1 NM_000138.4 +/. - c.7C>T r.(?) p.(Arg3Ter)


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