Assay Details
Target Gene Details
Entrez Gene ID: | 5984 |
Gene Name: | replication factor C subunit 4 |
Gene Aliases: |
A1, RFC37 |
Location: |
Chr.3:186789892-186806695 on Build GRCh38 |
Assay Gene Location: | Within Intron 3 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| RFC4 | NM_002916.3 | NP_002907.1 | ||
| NM_181573.2 | NP_853551.1 | |||
| AK297282.1 | ||||
| BC017452.1 | AAH17452.1 | |||
| BC024022.1 | AAH24022.1 | |||
| BM837975.1 | ||||
| BT006987.1 | AAP35633.1 | |||
| CR536561.1 | CAG38798.1 | |||
| CX788139.1 | ||||
| DA359927.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv1001111 | Chr.3:186796249 - 187014891 on Build GRCh38 | Gain |
|
| esv3893839 | Chr.3:186785646 - 186958667 on Build GRCh38 | Gain |
|
| esv2759206 | Chr.3:186619345 - 186849537 on Build GRCh38 | Loss |
|
| dgv5005n100 | Chr.3:186709551 - 186836503 on Build GRCh38 | Gain |
|
| nsv1012615 | Chr.3:186676249 - 186950429 on Build GRCh38 | Gain |
|
| esv34136 | Chr.3:186697095 - 187036942 on Build GRCh38 | Loss |
|
More Information
Additional Information:
For this assay, SNP(s) [rs73886088] 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: |
|

Genomic Map