Assay Details
Target Gene Details
Entrez Gene ID: | 85477 |
Gene Name: | scinderin |
Gene Aliases: |
- |
Location: |
Chr.7:12570349-12653603 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 2 - Exon 3 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| SCIN | NM_001112706.2 | NP_001106177.1 | ||
| AB067492.1 | BAB67798.1 | |||
| AF276507.1 | AAK60494.1 | |||
| AK075123.1 | BAC11416.1 | |||
| AK290363.1 | ||||
| BC021090.1 | AAH21090.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| dgv6274n100 | Chr.7:12490865 - 12683322 on Build GRCh38 | Loss |
|
| nsv1018053 | Chr.7:12540928 - 12593371 on Build GRCh38 | Gain |
|
| esv3576293 | Chr.7:12565967 - 12601226 on Build GRCh38 | Gain |
|
More Information
Additional Information:
For this assay, SNP(s) [rs77923354] 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