Product Details
- SNP ID
-
rs145386095
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.X:130350719 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- TATCTTCCACTATAGCCAATCCCAC[C/T]GATGTTCTAAAGGTAAGAGAGATAC
- Phenotype
-
MIM: 300242
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
SLC25A14
PubMed Links
Gene Details
- Gene
- SLC25A14
- Gene Name
- solute carrier family 25 member 14
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001282195.1 |
766 |
Silent Mutation |
ACC,ACT |
T162T |
NP_001269124.1 |
NM_001282196.1 |
766 |
Silent Mutation |
ACC,ACT |
T159T |
NP_001269125.1 |
NM_001282197.1 |
766 |
Silent Mutation |
ACC,ACT |
T159T |
NP_001269126.1 |
NM_001282198.1 |
766 |
Silent Mutation |
ACC,ACT |
T127T |
NP_001269127.1 |
XM_005262489.4 |
766 |
Silent Mutation |
ACC,ACT |
T61T |
XP_005262546.1 |
XM_011531402.2 |
766 |
Silent Mutation |
ACC,ACT |
T171T |
XP_011529704.1 |
XM_011531403.1 |
766 |
Intron |
|
|
XP_011529705.1 |
XM_017029936.1 |
766 |
Silent Mutation |
ACC,ACT |
T127T |
XP_016885425.1 |
XM_017029937.1 |
766 |
Silent Mutation |
ACC,ACT |
T171T |
XP_016885426.1 |
XM_017029938.1 |
766 |
Silent Mutation |
ACC,ACT |
T162T |
XP_016885427.1 |
XM_017029939.1 |
766 |
Silent Mutation |
ACC,ACT |
T159T |
XP_016885428.1 |
XM_017029940.1 |
766 |
Silent Mutation |
ACC,ACT |
T61T |
XP_016885429.1 |
XM_017029941.1 |
766 |
Silent Mutation |
ACC,ACT |
T18T |
XP_016885430.1 |
XM_017029942.1 |
766 |
Silent Mutation |
ACC,ACT |
T18T |
XP_016885431.1 |
XM_017029943.1 |
766 |
Intron |
|
|
XP_016885432.1 |
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