Variant #0000763699 (NC_000002.11:g.48040385_48040391del, FBXO11(NM_001190274.1):c.2211_2217del)

Individual ID 00362014
Chromosome 2
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method ACMG
Clinical classification likely pathogenic (dominant)
DNA change (genomic) (Relative to hg19 / GRCh37) g.48040385_48040391del
DNA change (hg38) g.47813246_47813252del
Published as -
ISCN -
DB-ID FBXO11_000046
Variant remarks ACMG: PVS1, PM2_SUP
Reference -
ClinVar ID -
dbSNP ID -
Origin Germline/De novo (untested)
Segregation ?
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner Andreas Laner
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Andreas Laner
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FBXO11 NM_001190274.1 +?/. - c.2211_2217del r.(?) p.(Ile737Metfs*30)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000363242 DNA SEQ-NG-I - - FBXO11 1 Andreas Laner