Genomic Map
Back To TopAssay Details
Target Gene Details
Entrez Gene ID: | 392 |
Gene Name: | Rho GTPase activating protein 1 |
Gene Aliases: |
CDC42GAP, RHOGAP, RHOGAP1, p50rhoGAP |
Location: |
Chr.11:46677075-46700665 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 8 - Exon 8 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| ARHGAP1 | NM_004308.3 | NP_004299.1 | ||
| XM_011520095.1 | XP_011518397.1 | |||
| XM_017017720.1 | XP_016873209.1 | |||
| AK298562.1 | ||||
| BC018118.1 | AAH18118.1 | |||
| U02570.1 | AAA16142.1 | |||
| U62794.1 | AAB66594.1 | |||
| Z23024.1 | CAA80560.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| esv3626191 | Chr.11:46651662 - 46681651 on Build GRCh38 | Gain |
 ATG13
ARHGAP1
|
Back To TopMore Information
Additional Information:
For this assay, SNP(s) [rs112112676] 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:
Back To Top