Variant #0000983709 (NC_000019.9:g.8130867G>T, NM_032447.3:c.8366C>A (FBN3))

Chromosome 19
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.8130867G>T
DNA change (hg38) -
Published as FBN3(NM_032447.5):c.8366C>A (p.(Pro2789Gln))
ISCN -
DB-ID FBN3_000072 See all 2 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) 0.00276 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +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     
CCL25 NM_005624.3 -?/. - c.*3758G>T r.(=) p.(=)
FBN3 NM_032447.3 -?/. - c.8366C>A r.(?) p.(Pro2789Gln)


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