Assay Details
Target Gene Details
Entrez Gene ID: | 283600 |
Gene Name: | solute carrier family 25 member 47 |
Gene Aliases: |
C14orf68, HDMCP, HMFN1655 |
Location: |
Chr.14:100323342-100330378 on Build GRCh38 |
Assay Gene Location: | Within Exon 6 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
SLC25A47 | NM_207117.2 | 6 | 1641 | NP_997000.2 |
AB073385.1 | 7 | 1565 | BAD38636.1 | |
AK092001.1 | 7 | 1551 | ||
AY569438.1 | 6 | 1641 | AAS80155.1 | |
BX248260.1 | CAD62588.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv832875 | Chr.14:100192592 - 100368905 on Build GRCh38 | Loss |
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More Information
Additional Information:
For this assay, SNP(s) [rs74085049] 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:
Gene Ontology Categories:
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