Assay Details
Target Gene Details
Entrez Gene ID: | 158234 |
Gene Name: | tRNA methyltransferase 10B |
Gene Aliases: |
RG9MTD3, bA3J10.9 |
Location: |
Chr.9:37753204-37780459 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
TRMT10B | XM_011517735.2 | XP_011516037.1 | ||
XM_011517736.2 | XP_011516038.1 | |||
XM_011517738.2 | XP_011516040.1 | |||
XM_011517739.2 | XP_011516041.1 | |||
XM_011517742.1 | XP_011516044.1 | |||
XM_011517743.2 | XP_011516045.1 | |||
XM_017014313.1 | XP_016869802.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv831552 | Chr.9:37693652 - 37859980 on Build GRCh38 | Gain | DCAF10 EXOSC3 FRMPD1 TRMT10B LOC105376037 |
esv3891658 | Chr.9:37689626 - 37790130 on Build GRCh38 | Gain | EXOSC3 FRMPD1 TRMT10B LOC105376037 |
nsv469813 | Chr.9:37628200 - 37777281 on Build GRCh38 | Loss | FRMPD1 TRMT10B RAB1C |
More Information
Additional Information:
For this assay, SNP(s) [rs149156654,rs78591290] 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 |