Genomic variant #0000715132

Individual ID 00000003
Chromosome 17
Allele Unknown
Affects function (reported) Not classified
Affects function (concluded) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.69016174_69016178del
Reference dbSNP
DB-ID ABCA9_000048
Frequency 0.005155
Allele Count 1
Allele Number 194
Depth 291
Average frequency (large NGS studies) Variant not found in online data sets
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     
ABCA9 NM_080283.3 ./.
ABCA9-AS1 NR_126414.1 ./.
ABCA9 XM_005256934.3 ./.
ABCA9 XM_005256937.3 ./.
ABCA9 XM_006721633.2 ./.
ABCA9 XM_011524186.1 ./.
ABCA9 XM_011524187.1 ./.



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000003 DNA SEQ-NG-I - 624137 Admin