Genomic variant #0000599327

Individual ID 00000001
Chromosome 19
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.1058176A>G
Reference -
DB-ID ABCA7_000003
dbSNP ID rs4147918
Frequency 0.0544
Homozygous 6
Heterozygote 25
Average frequency (large NGS studies) Retrieve
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ABCA7 NM_019112.3 ./. - c.5056A>G - -



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000001 DNA arrayCNV - 904861 Admin