Variant #0000036628 (NC_000022.10:g.19711814del, GP1BB(NM_000407.4):c.448del)

Individual ID 00016777
Chromosome 22
Allele Parent #2
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic (recessive)
DNA change (genomic) (Relative to hg19 / GRCh37) g.19711814del
DNA change (hg38) g.19724291del
Published as -
ISCN -
DB-ID GP1BB_000029
Variant remarks -
Reference PubMed: Kunishima 2006
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner Anna Savoia
Database submission license No license selected
Created by Anna Savoia
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GP1BB NM_000407.4 +/. 2 c.448del r.(?) p.(Ala150Argfs*43)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000016739 DNA ? - - GP1BB 2 Anna Savoia