Assay Details
Target Gene Details
Entrez Gene ID: | 399694 |
Gene Name: | SHC adaptor protein 4 |
Gene Aliases: |
RaLP, SHCD |
Location: |
Chr.15:48823737-48963444 on Build GRCh38 |
Assay Gene Location: | Within Intron 10 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
SHC4 | NM_203349.3 | NP_976224.3 | ||
XM_005254375.3 | XP_005254432.1 | |||
AK124916.1 | ||||
AK125762.1 | ||||
AK302156.1 | ||||
AY358250.1 | AAQ88617.1 | |||
AY464565.1 | AAR19363.1 | |||
BC033907.2 | AAH33907.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv833001 | Chr.15:48751446 - 48912568 on Build GRCh38 | Gain | EID1 CEP152 SHC4 |
More Information
Additional Information:
For this assay, SNP(s) [rs75698533] 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 |