Genomic variant #0000579559

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.21882949T>G
Reference dbSNP
DB-ID ABCC9_000031
Frequency 0.281
Allele Count 59
Allele Number 210
Depth 992
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