Assay Details
Target Gene Details
Entrez Gene ID: | 91646 |
Gene Name: | tudor domain containing 12 |
Gene Aliases: |
ECAT8 |
Location: |
Chr.19:32719773-32829580 on Build GRCh38 |
Assay Gene Location: | Within Intron 5 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
TDRD12 | NM_001110822.1 | NP_001104292.1 | ||
XM_011527471.2 | XP_011525773.1 | |||
XM_011527472.2 | XP_011525774.1 | |||
XM_011527473.2 | XP_011525775.1 | |||
XM_011527474.2 | XP_011525776.1 | |||
XM_011527475.2 | XP_011525777.1 | |||
XM_011527476.2 | XP_011525778.1 | |||
XM_017027458.1 | XP_016882947.1 | |||
AB211063.1 | BAD95490.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv1067189 | Chr.19:32712741 - 32816579 on Build GRCh38 | Loss | TDRD12 NUDT19 |
nsv458535 | Chr.19:32716739 - 32824007 on Build GRCh38 | Loss | TDRD12 |
More Information
Additional Information:
For this assay, SNP(s) [rs147916161] are located under a primer or probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.
Set Membership: |
Intragenic Intronic Non-exonic DGV Variation |