Product Details
- SNP ID
-
rs200438932
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
1
- Location
-
Chr.1:156200301 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- TGAGAAAATGGGCCGCTTTCAGGTG[A/C]GGGGGAACCCAGAGGGACAAGGGGT
- Phenotype
-
MIM: 610824
- Polymorphism
- A/C, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
SLC25A44
PubMed Links
Gene Details
- Gene
- SLC25A44
- Gene Name
- solute carrier family 25 member 44
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_001286184.1 |
1341 |
Silent Mutation |
AGG,CGG |
R152R |
NP_001273113.1 |
| NM_014655.3 |
1341 |
Silent Mutation |
AGG,CGG |
R152R |
NP_055470.1 |
| XM_006711657.3 |
1341 |
Silent Mutation |
AGG,CGG |
R152R |
XP_006711720.1 |
| XM_011510180.1 |
1341 |
Silent Mutation |
AGG,CGG |
R152R |
XP_011508482.1 |
| XM_011510181.1 |
1341 |
Silent Mutation |
AGG,CGG |
R152R |
XP_011508483.1 |
| XM_017002904.1 |
1341 |
Silent Mutation |
AGG,CGG |
R152R |
XP_016858393.1 |
| XM_017002905.1 |
1341 |
Silent Mutation |
AGG,CGG |
R152R |
XP_016858394.1 |
| XM_017002906.1 |
1341 |
Silent Mutation |
AGG,CGG |
R152R |
XP_016858395.1 |
| XM_017002907.1 |
1341 |
Silent Mutation |
AGG,CGG |
R152R |
XP_016858396.1 |
| XM_017002908.1 |
1341 |
Silent Mutation |
AGG,CGG |
R152R |
XP_016858397.1 |
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