Assay Details
Target Gene Details
Entrez Gene ID: | 64121 |
Gene Name: | Ras related GTP binding C |
Gene Aliases: |
GTR2, RAGC, TIB929 |
Location: |
Chr.1:38838197-38859823 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 1 - Exon 1 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
RRAGC | NM_001271851.1 | NP_001258780.1 | ||
NM_022157.3 | NP_071440.1 | |||
AF272035.1 | AAG32662.1 | |||
AF323609.1 | AAG45221.1 | |||
AK298788.1 | ||||
AK315791.1 | ||||
BC016668.1 | AAH16668.1 | |||
BG717489.1 | ||||
BI461665.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv1078344 | Chr.1:38859427 - 38859828 on Build GRCh38 | Deletion | RRAGC |
More Information
Additional Information:
For this assay, SNP(s) [rs112925356] 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 Non-exonic DGV Variation |