Variant #0000276676 (NC_000014.8:g.92403294C>T, FBLN5(NM_006329.3):c.376G>A)

Chromosome 14
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.92403294C>T
DNA change (hg38) g.91936950C>T
Published as FBLN5(NM_006329.3):c.376G>A (p.(Val126Met)), FBLN5(NM_006329.4):c.376G>A (p.V126M)
ISCN -
DB-ID FBLN5_000008 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) 0.00185 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FBLN5 NM_006329.3 -?/. - c.376G>A r.(?) p.(Val126Met)