Product Details
- SNP ID
-
rs73015592
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.2:164898473 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- TACTAATATTTAAAGTAGAAAGTTG[C/T]GTTGTCTGCTGAACATGAGACTCTG
- Phenotype
-
MIM: 616526
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
SLC38A11
PubMed Links
Gene Details
- Gene
- SLC38A11
- Gene Name
- solute carrier family 38 member 11
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_001199148.1 |
1830 |
Silent Mutation |
ACA,ACG |
T395T |
NP_001186077.1 |
| NM_173512.2 |
1830 |
Silent Mutation |
ACA,ACG |
T373T |
NP_775783.1 |
| XM_005246350.4 |
1830 |
Silent Mutation |
ACA,ACG |
T451T |
XP_005246407.1 |
| XM_006712337.3 |
1830 |
Silent Mutation |
ACA,ACG |
T397T |
XP_006712400.1 |
| XM_011510737.2 |
1830 |
Silent Mutation |
ACA,ACG |
T429T |
XP_011509039.1 |
| XM_011510742.2 |
1830 |
Silent Mutation |
ACA,ACG |
T256T |
XP_011509044.1 |
| XM_017003455.1 |
1830 |
Silent Mutation |
ACA,ACG |
T477T |
XP_016858944.1 |
| XM_017003456.1 |
1830 |
Silent Mutation |
ACA,ACG |
T455T |
XP_016858945.1 |
| XM_017003457.1 |
1830 |
Silent Mutation |
ACA,ACG |
T452T |
XP_016858946.1 |
| XM_017003458.1 |
1830 |
Silent Mutation |
ACA,ACG |
T421T |
XP_016858947.1 |
| XM_017003459.1 |
1830 |
Silent Mutation |
ACA,ACG |
T399T |
XP_016858948.1 |
| XM_017003460.1 |
1830 |
Intron |
|
|
XP_016858949.1 |
| XM_017003461.1 |
1830 |
Intron |
|
|
XP_016858950.1 |
| XM_017003462.1 |
1830 |
Intron |
|
|
XP_016858951.1 |
| XM_017003463.1 |
1830 |
Silent Mutation |
ACA,ACG |
T329T |
XP_016858952.1 |
| XM_017003464.1 |
1830 |
Silent Mutation |
ACA,ACG |
T282T |
XP_016858953.1 |
| XM_017003465.1 |
1830 |
Silent Mutation |
ACA,ACG |
T282T |
XP_016858954.1 |
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