Genomic variant #0000040201

Individual ID 00019770
Chromosome 2
Allele Both (homozygous)
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.215851290T>C
DNA change (hg38) g.214986566T>C
Published as -
ISCN -
DB-ID ABCA12_000055 See all 6 reported entries
Variant remarks -
Reference PubMed: Lefevre 2003
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation yes
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (large NGS studies) 8.0E-5 View details
Owner Marianne Vos (LOVD-team)




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

ClassClinical     

RNA change     

Protein     
ABCA12 NM_173076.2 +/. 28 c.4139A>G - r.(?) p.(Asn1380Ser)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000019755 DNA SEQ ? - ABCA12 1 Marianne Vos (LOVD-team)