Variant #0001070808 (NC_000019.9:g.1055908del, NM_019112.3:c.4208del (ABCA7))

Chromosome 19
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.1055908del
DNA change (hg38) -
Published as -
ISCN -
DB-ID chr19_008797
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs538591288
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00094 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2026-03-16 14:03:01 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ABCA7 NM_019112.3 +?/. - c.4208del r.(?) p.(Leu1403ArgfsTer7)


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