Genomic variant #0000439808

Individual ID 00000003
Chromosome 7
Allele Unknown
Affects function (reported) Not classified
Affects function (concluded) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.48274770G>A
Reference -
DB-ID ABCA13_000071
Frequency 0.004717
Allele Count 1
Allele Number 212
Depth 3807
Average frequency (large NGS studies) Variant not found in online data sets
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     
ABCA13 NM_152701.4 ./.
ABCA13 XM_011515130.1 ./.
ABCA13 XM_011515131.1 ./.
ABCA13 XM_011515132.1 ./.
ABCA13 XM_011515133.1 ./.
ABCA13 XM_011515134.1 ./.
ABCA13 XM_011515135.1 ./.
ABCA13 XM_011515136.1 ./.
ABCA13 XM_011515137.1 ./.
ABCA13 XM_011515138.1 ./.
ABCA13 XM_011515139.1 ./.
ABCA13 XM_011515140.1 ./.
ABCA13 XM_011515141.1 ./.
ABCA13 XM_011515142.1 ./.
ABCA13 XM_011515143.1 ./.
ABCA13 XM_011515144.1 ./.
ABCA13 XM_011515145.1 ./.
ABCA13 XM_011515146.1 ./.
ABCA13 XM_011515147.1 ./.
ABCA13 XM_011515148.1 ./.
ABCA13 XM_011515149.1 ./.



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000003 DNA SEQ-NG-I - 624137 Admin