Assay Details
Target Gene Details
Entrez Gene ID: | 112611 |
Gene Name: | RWD domain containing 2A |
Gene Aliases: |
RWDD2, dJ747H23.2 |
Location: |
Chr.6:83193313-83198935 on Build GRCh38 |
Assay Gene Location: | Within Exon 3 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
RWDD2A | NM_001322335.1 | 3 | 3439 | NP_001309264.1 |
NM_001322336.1 | 4 | 3750 | NP_001309265.1 | |
NM_001322337.1 | 4 | 3735 | NP_001309266.1 | |
NM_001322339.1 | 4 | 3531 | NP_001309268.1 | |
NM_033411.4 | 3 | 3658 | NP_219479.2 | |
XM_017010222.1 | 3 | 4241 | XP_016865711.1 | |
XM_017010223.1 | 3 | 4016 | XP_016865712.1 | |
AJ420581.1 | 1 | 1797 | ||
AW197622.1 | 1 | 166 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv1026095 | Chr.6:83040907 - 83209453 on Build GRCh38 | Gain |
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More Information
Additional Information:
For this assay, SNP(s) [rs73749746] 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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Panther Classification:
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