Genomic variant #0000345849

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.183988842A>C
Reference dbSNP
DB-ID ABCC5_000044
Frequency 0.594
Allele Count 126
Allele Number 212
Depth 2365
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