Assay Details
Target Gene Details
Entrez Gene ID: | 8732 |
Gene Name: | RNA guanylyltransferase and 5'-phosphatase |
Gene Aliases: |
CAP1A, HCE, HCE1, hCAP |
Location: |
Chr.6:88609897-88963716 on Build GRCh38 |
Assay Gene Location: | Within Intron 17 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
RNGTT | NM_001286426.1 | NP_001273355.1 | ||
NM_001286428.1 | NP_001273357.1 | |||
NM_003800.4 | NP_003791.3 | |||
XM_017011401.1 | XP_016866890.1 | |||
AB009022.1 | BAA25894.1 | |||
AB009023.1 | BAA25895.1 | |||
AB012142.1 | BAA25198.1 | |||
AF025654.1 | AAB91559.1 | |||
AK295719.1 | ||||
AK299777.1 | ||||
AK312407.1 | ||||
BC019954.1 | AAH19954.1 | |||
BX537450.1 | CAD97693.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv5390 | Chr.6:88613645 - 88660252 on Build GRCh38 | Deletion | RNGTT |
dgv6087n100 | Chr.6:88552751 - 88940524 on Build GRCh38 | Gain | RNGTT |
More Information
Additional Information:
For this assay, SNP(s) [rs72458928] 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 |