Genomic variant #0000710584

Individual ID 00000003
Chromosome 17
Allele Unknown
Affects function (reported) Not classified
Affects function (concluded) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.50672871del
Reference dbSNP
DB-ID ABCC3_000024
Frequency 0.064
Allele Count 11
Allele Number 172
Depth 369
Average frequency (large NGS studies) Variant not found in online data sets
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     
ABCC3 NM_001144070.1 ./.
ABCC3 NM_003786.3 ./.
ABCC3 XM_005257763.2 ./.
ABCC3 XM_011525422.1 ./.
ABCC3 XM_011525423.1 ./.
ABCC3 XM_011525424.1 ./.
ABCC3 XM_011525425.1 ./.



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000003 DNA SEQ-NG-I - 624137 Admin