Genomic variant #0000736244

Individual ID 00000003
Chromosome 19
Allele Unknown
Affects function (reported) Not classified
Affects function (concluded) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.1047017T>C
Reference dbSNP
DB-ID ABCA7_000066
Frequency 0.004717
Allele Count 1
Allele Number 212
Depth 4677
Average frequency (large NGS studies) Variant not found in online data sets
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     
ABCA7 NM_019112.3 ./.
ABCA7 XM_006722616.1 ./.
ABCA7 XM_006722617.2 ./.
ABCA7 XM_006722618.2 ./.
ABCA7 XM_011527628.1 ./.
ABCA7 XM_011527629.1 ./.
ABCA7 XM_011527630.1 ./.
ABCA7 XM_011527631.1 ./.
ABCA7 XM_011527632.1 ./.
ABCA7 XM_011527633.1 ./.
ABCA7 XM_011527634.1 ./.
ABCA7 XM_011527635.1 ./.
ABCA7 XM_011527636.1 ./.



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000003 DNA SEQ-NG-I - 624137 Admin