Assay Details
Target Gene Details
Entrez Gene ID: | 55238 |
Gene Name: | solute carrier family 38 member 7 |
Gene Aliases: |
SNAT7 |
Location: |
Chr.16:58665109-58684777 on Build GRCh38 |
Assay Gene Location: | Within Exon 12 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
SLC38A7 | NM_001308384.1 | 8 | 2230 | NP_001295313.1 |
NM_018231.2 | 12 | 2165 | NP_060701.1 | |
XM_017023393.1 | 11 | 2646 | XP_016878882.1 | |
XM_017023394.1 | 9 | 1738 | XP_016878883.1 | |
XM_017023395.1 | 11 | 1941 | XP_016878884.1 | |
XM_017023396.1 | 10 | 1793 | XP_016878885.1 | |
AK001677.1 | 12 | 2158 | BAA91830.1 | |
BC001961.1 | 11 | 2114 | AAH01961.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv510686 | Chr.16:58612215 - 58731990 on Build GRCh38 | Deletion | CNOT1 SLC38A7 GOT2 |
esv2758650 | Chr.16:58545101 - 58842133 on Build GRCh38 | Loss | CNOT1 SNORA46 SNORA50A SLC38A7 GOT2 |
nsv528513 | Chr.16:58638859 - 58683970 on Build GRCh38 | Loss | SLC38A7 |
More Information
Set Membership: |
Intragenic Exonic DGV Variation |