Product Details
- SNP ID
-
rs74435752
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.12:7817861 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CAGAGGGGAAGAGCAATCCGACTAG[A/G]AAGTTGGAGGTCCAGTTGGAGCAGC
- Phenotype
-
MIM: 611039
- Polymorphism
- A/G, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
SLC2A14
PubMed Links
Gene Details
- Gene
- SLC2A14
- Gene Name
- solute carrier family 2 member 14
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_001286233.1 |
1723 |
Silent Mutation |
TTC,TTT |
F438F |
NP_001273162.1 |
| NM_001286234.1 |
1723 |
Silent Mutation |
TTC,TTT |
F415F |
NP_001273163.1 |
| NM_001286235.1 |
1723 |
Silent Mutation |
TTC,TTT |
F415F |
NP_001273164.1 |
| NM_001286236.1 |
1723 |
Silent Mutation |
TTC,TTT |
F329F |
NP_001273165.1 |
| NM_001286237.1 |
1723 |
Intron |
|
|
NP_001273166.1 |
| NM_153449.3 |
1723 |
Silent Mutation |
TTC,TTT |
F438F |
NP_703150.1 |
| XM_005253315.3 |
1723 |
Intron |
|
|
XP_005253372.1 |
| XM_005253317.4 |
1723 |
Silent Mutation |
TTC,TTT |
F415F |
XP_005253374.1 |
| XM_011520562.1 |
1723 |
Silent Mutation |
TTC,TTT |
F415F |
XP_011518864.1 |
| XM_011520563.2 |
1723 |
Intron |
|
|
XP_011518865.1 |
| XM_011520564.2 |
1723 |
Silent Mutation |
TTC,TTT |
F329F |
XP_011518866.1 |
| XM_011520565.2 |
1723 |
Silent Mutation |
TTC,TTT |
F329F |
XP_011518867.1 |
| XM_017018841.1 |
1723 |
Intron |
|
|
XP_016874330.1 |
| XM_017018842.1 |
1723 |
Intron |
|
|
XP_016874331.1 |
| XM_017018843.1 |
1723 |
Silent Mutation |
TTC,TTT |
F439F |
XP_016874332.1 |
| XM_017018844.1 |
1723 |
Intron |
|
|
XP_016874333.1 |
| XM_017018845.1 |
1723 |
Silent Mutation |
TTC,TTT |
F439F |
XP_016874334.1 |
| XM_017018846.1 |
1723 |
Intron |
|
|
XP_016874335.1 |
| XM_017018847.1 |
1723 |
Intron |
|
|
XP_016874336.1 |
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