Variant #0000724918 (NC_000014.8:g.92403402C>T, FBLN5(NM_006329.3):c.268G>A)

Chromosome 14
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.92403402C>T
DNA change (hg38) -
Published as FBLN5(NM_006329.3):c.268G>A (p.G90S), FBLN5(NM_006329.4):c.268G>A (p.G90S)
ISCN -
DB-ID FBLN5_000009 See all 4 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) 0.00039 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FBLN5 NM_006329.3 ?/. - c.268G>A r.(?) p.(Gly90Ser)