Assay Details
Target Gene Details
Entrez Gene ID: | 112495 |
Gene Name: | general transcription factor IIIC subunit 6 |
Gene Aliases: |
C6orf51, TFIIIC35, bA397G5.3 |
Location: |
Chr.6:110958560-110967888 on Build GRCh38 |
Assay Gene Location: | Within Intron 5 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
GTF3C6 | NM_138408.3 | NP_612417.1 | ||
AF361492.1 | AAL57217.1 | |||
AF361496.1 | AAL57221.1 | |||
AK057977.1 | BAB71624.1 | |||
BC011593.1 | AAH11593.1 | |||
BQ269752.1 | ||||
EF137904.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv1032572 | Chr.6:110800096 - 111060820 on Build GRCh38 | Gain | CDK19 AMD1 RPF2 GTF3C6 GSTM2P1 |
nsv1016001 | Chr.6:110959208 - 110988298 on Build GRCh38 | Gain | RPF2 GTF3C6 |
nsv830773 | Chr.6:110813116 - 110985229 on Build GRCh38 | Loss | CDK19 AMD1 RPF2 GTF3C6 |
nsv509148 | Chr.6:110947375 - 110967436 on Build GRCh38 | Insertion | GTF3C6 |
More Information
Additional Information:
For this assay, SNP(s) [rs73541347] 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 |