Hs06838977_cn

• Gene Symbol: TRMT10B
• Assay Reference Genome Location: Chr.9:37769488 on build GRCh38
• Cytoband: 9p13.2

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 7

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
TRMT10B	NM_001286950.1			NP_001273879.1
	NM_001286951.1			NP_001273880.1
	NM_001286952.1			NP_001273881.1
	NM_001286953.1			NP_001273882.1
	NM_001286954.1			NP_001273883.1
	NM_144964.3			NP_659401.2
	NR_104612.1
	XM_005251375.2			XP_005251432.1
	XM_005251379.2			XP_005251436.1
	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_017014313.1			XP_016869802.1
	AK056017.1			BAB71074.1
	AK092718.1			BAC03957.1
	AK294219.1
	AK295733.1
	AK304516.1
	AK315922.1
	BC012175.1
	BC057774.1			AAH57774.1
	CR986760.1

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 LOC105376037 EXOSC3 TRMT10B FRMPD1
esv3891658	Chr.9:37689626 - 37790130 on Build GRCh38	Gain	LOC105376037 EXOSC3 TRMT10B FRMPD1
nsv469813	Chr.9:37628200 - 37777281 on Build GRCh38	Loss	RAB1C TRMT10B FRMPD1

More Information

Additional Information:

For this assay, SNP(s) [rs78713199] 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

Panther Classification:

Molecular Function -

RNA methyltransferase

Gene Ontology Categories:

Process(es)

methylation

Function(s)

methyltransferase activity