Assay Details
Target Gene Details
Entrez Gene ID: | 22931 |
Gene Name: | RAB18, member RAS oncogene family |
Gene Aliases: |
RAB18LI1, WARBM3 |
Location: |
Chr.10:27504174-27542237 on Build GRCh38 |
Assay Gene Location: | Within Exon 8 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| RAB18 | NM_001256410.1 | 8 | 1651 | NP_001243339.1 |
| NM_001256411.1 | 6 | 1497 | NP_001243340.1 | |
| NM_001256412.1 | 5 | 1372 | NP_001243341.1 | |
| NM_001256415.1 | 6 | 1492 | NP_001243344.1 | |
| NM_021252.4 | 7 | 1564 | NP_067075.1 | |
| NR_046172.1 | 6 | 1502 | ||
| AB209698.1 | 3 | 6326 | BAD92935.1 | |
| AK001555.1 | 7 | 1368 | ||
| AK223153.1 | 7 | 1391 | BAD96873.1 | |
| AK295443.1 | 5 | 1242 | ||
| AK299457.1 | 6 | 1368 | ||
| AL136734.1 | 7 | 1417 | CAB66668.1 | |
| AY574034.1 | 8 | 1540 | AAU08232.1 | |
| BC015014.2 | 7 | 1418 | AAH15014.1 | |
| BC029350.1 | 7 | 1434 | AAH29350.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv1045257 | Chr.10:27283511 - 27638017 on Build GRCh38 | Gain |
|
| nsv550241 | Chr.10:27280592 - 27736842 on Build GRCh38 | Gain |
|
| nsv8614 | Chr.10:27215558 - 27539477 on Build GRCh38 | Loss |
|
| esv3622708 | Chr.10:27138085 - 27696800 on Build GRCh38 | Gain |
|
| esv2734606 | Chr.10:27447765 - 29432048 on Build GRCh38 | Deletion |
|
More Information
Additional Information:
For this assay, SNP(s) [rs76051289] 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: |
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Genomic Map