Genomic variant #0000918243

Individual ID 00000001
Chromosome 19
Allele Unknown
Affects function (reported) Not classified
Affects function (concluded) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.1057863A>T
Reference dbSNP
DB-ID ABCA7_000002
Frequency 0.848
Average frequency (large NGS studies) 0.10703 View details
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ABCA7 NM_019112.3 ./. - c.4881-52A>T - -



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000001 DNA arraySNP - 905346 Admin