Genomic variant #0000710562

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.50659029G>C
Reference dbSNP
DB-ID ABCC3_000057
Frequency 0.004762
Allele Count 1
Allele Number 210
Depth 413
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