Assay Details
Target Gene Details
Entrez Gene ID: | 257106 |
Gene Name: | Rho GTPase activating protein 30 |
Gene Aliases: |
- |
Location: |
Chr.1:161046942-161069971 on Build GRCh38 |
Assay Gene Location: | Within Exon 12 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
ARHGAP30 | NM_001025598.1 | 12 | 3699 | NP_001020769.1 |
NM_001287600.1 | 11 | 3554 | NP_001274529.1 | |
NM_001287602.1 | 8 | 3168 | NP_001274531.1 | |
NM_181720.2 | 13 | 3066 | NP_859071.2 | |
XM_005245070.2 | 12 | 3528 | XP_005245127.1 | |
XM_005245073.3 | 10 | 3452 | XP_005245130.1 | |
XM_011509391.2 | 11 | 3530 | XP_011507693.1 | |
XM_017000960.1 | 11 | 3297 | XP_016856449.1 | |
AK126116.1 | BAC86447.1 | |||
AK126163.1 | 8 | 3168 | ||
AK160366.1 | 12 | 3674 | ||
AL832852.1 | 10 | 3134 | ||
AL833477.1 | 1 | 1842 | ||
BC053688.1 | 13 | 2762 | AAH53688.1 | |
BX537846.1 | 10 | 4135 | CAD97855.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv3221 | Chr.1:161038385 - 161083189 on Build GRCh38 | Deletion | ARHGAP30 NECTIN4 USF1 TSTD1 |
More Information
Additional Information:
For this assay, SNP(s) [rs75570999] 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 Exonic DGV Variation |