Genomic variant #0000579535

Individual ID 00000003
Chromosome 12
Allele Unknown
Affects function (reported) Not classified
Affects function (concluded) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.21845681C>T
Reference -
DB-ID ABCC9_000029
Frequency 0.004717
Allele Count 1
Allele Number 212
Depth 3755
Average frequency (large NGS studies) Variant not found in online data sets
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     
ABCC9 NM_005691.3 ./.
ABCC9 NM_020297.3 ./.
ABCC9 XM_005253284.2 ./.
ABCC9 XM_005253286.2 ./.
ABCC9 XM_005253287.3 ./.
ABCC9 XM_005253288.2 ./.
ABCC9 XM_005253289.2 ./.
ABCC9 XM_005253290.2 ./.
ABCC9 XM_006719025.2 ./.
ABCC9 XM_011520545.1 ./.



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000003 DNA SEQ-NG-I - 624137 Admin