Variant #0000892121 (NC_000015.9:g.48764870A>C, NM_000138.4:c.4214T>G (FBN1))

Chromosome 15
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.48764870A>C
DNA change (hg38) -
Published as FBN1(NM_000138.4):c.4214T>G (p.L1405R, p.(Leu1405Arg)), FBN1(NM_000138.5):c.4214T>G (p.L1405R)
ISCN -
DB-ID FBN1_000558 See all 8 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) 0.00011 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2022-11-01 13:41:49 +01:00 (CET)
Date last edited 2025-02-07 18:57:27 +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.4214T>G r.(?) p.(Leu1405Arg)


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