Genomic Map
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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
|
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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
|
Panther Classification:
Gene Ontology Categories:
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