Genomic variant #0000345845

Individual ID 00000003
Chromosome 3
Allele Unknown
Affects function (reported) Not classified
Affects function (concluded) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.183984897G>A
Reference -
DB-ID ABCC5_000036
Frequency 0.004717
Allele Count 1
Allele Number 212
Depth 2213
Average frequency (large NGS studies) Variant not found in online data sets
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     
ABCC5 NM_001023587.1 ./.
ABCC5 NM_005688.2 ./.
ABCC5 XM_005247058.3 ./.
ABCC5 XM_005247059.3 ./.
ABCC5 XM_011512314.1 ./.
ABCC5 XM_011512315.1 ./.
ABCC5 XM_011512316.1 ./.



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000003 DNA SEQ-NG-I - 624137 Admin