Assay Details
Target Gene Details
Entrez Gene ID: | 83452 |
Gene Name: | RAB33B, member RAS oncogene family |
Gene Aliases: |
SMC2 |
Location: |
Chr.4:139453232-139475916 on Build GRCh38 |
Assay Gene Location: | Within Intron 2 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
RAB33B | NM_031296.2 | NP_112586.1 | ||
XM_011532299.1 | XP_011530601.1 | |||
AF350420.1 | AAL83916.1 | |||
AK313685.1 | ||||
AL136904.1 | CAB66838.1 | |||
BC036064.1 | AAH36064.1 | |||
BC111977.1 | AAI11978.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv830085 | Chr.4:139393507 - 139586168 on Build GRCh38 | Loss | SETD7 LOC105377450 LOC101927451 RAB33B |
nsv830084 | Chr.4:139326103 - 139478732 on Build GRCh38 | Loss | NAA15 LOC105377450 LOC101927451 RAB33B |
nsv1023892 | Chr.4:139377986 - 139483575 on Build GRCh38 | Gain | NAA15 LOC105377450 LOC101927451 RAB33B |
More Information
Additional Information:
For this assay, SNP(s) [rs148238737] 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 Intronic Non-exonic DGV Variation |