Variant #0000040156 (NC_000002.11:g.215843040_215843043del, ABCA12(NM_173076.2):c.5126_5128+1del)

Individual ID 00019735
Chromosome 2
Allele Parent #1
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.215843040_215843043del
DNA change (hg38) g.214978316_214978319del
Published as 5125_5128delGATG
ISCN -
DB-ID ABCA12_000028
Variant remarks no variant found 2nd chromosome
Reference PubMed: Thomas 2008
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation yes
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner Marianne Vos (LOVD-team)
Database submission license No license selected
Created by Marianne Vos (LOVD-team)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ABCA12 NM_173076.2 +/. 33_33i c.5126_5128+1del r.spl p.?



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000019720 DNA SEQ blood - ABCA12 1 Marianne Vos (LOVD-team)