Variant #0000040184 (NC_000002.11:g.215831608G>A, ABCA12(NM_173076.2):c.5848C>T)

Individual ID 00019756
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.215831608G>A
DNA change (hg38) g.214966884G>A
Published as Arg1950X
ISCN -
DB-ID ABCA12_000042 See all 2 reported entries
Variant remarks -
Reference PubMed: Sakai 2009
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation ?
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
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 +/. 39 c.5848C>T r.(?) p.(Arg1950*)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000019741 DNA SEQ ? - ABCA12 2 Marianne Vos (LOVD-team)