Product Details
- SNP ID
-
rs113577701
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.15:84888838 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GATCAGGAGCAGCTGGAGCGAGGCG[A/G]CGCCGAAGCCCTTCTCCAGATGGTA
- Phenotype
-
MIM: 606207
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
SLC28A1
PubMed Links
Gene Details
- Gene
- SLC28A1
- Gene Name
- solute carrier family 28 member 1
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001287761.1 |
369 |
Missense Mutation |
ACG,GCG |
T55A |
NP_001274690.1 |
NM_001287762.1 |
369 |
Missense Mutation |
ACG,GCG |
T55A |
NP_001274691.1 |
NM_001321721.1 |
369 |
Missense Mutation |
ACG,GCG |
T55A |
NP_001308650.1 |
NM_001321722.1 |
369 |
Missense Mutation |
ACG,GCG |
T55A |
NP_001308651.1 |
NM_004213.4 |
369 |
Missense Mutation |
ACG,GCG |
T55A |
NP_004204.3 |
NM_201651.2 |
369 |
Missense Mutation |
ACG,GCG |
T55A |
NP_964014.1 |
XM_011522203.2 |
369 |
Missense Mutation |
ACG,GCG |
T55A |
XP_011520505.1 |
XM_011522204.2 |
369 |
Missense Mutation |
ACG,GCG |
T55A |
XP_011520506.1 |
XM_011522205.2 |
369 |
Missense Mutation |
ACG,GCG |
T55A |
XP_011520507.1 |
XM_011522206.2 |
369 |
Missense Mutation |
ACG,GCG |
T55A |
XP_011520508.1 |
XM_011522207.2 |
369 |
Missense Mutation |
ACG,GCG |
T55A |
XP_011520509.1 |
XM_011522208.2 |
369 |
Intron |
|
|
XP_011520510.1 |
XM_011522209.2 |
369 |
Missense Mutation |
ACG,GCG |
T55A |
XP_011520511.1 |
XM_011522210.2 |
369 |
Missense Mutation |
ACG,GCG |
T55A |
XP_011520512.1 |
XM_011522211.2 |
369 |
Intron |
|
|
XP_011520513.1 |
XM_011522212.1 |
369 |
Missense Mutation |
ACG,GCG |
T55A |
XP_011520514.1 |
XM_011522214.2 |
369 |
Missense Mutation |
ACG,GCG |
T55A |
XP_011520516.1 |
XM_011522215.2 |
369 |
Missense Mutation |
ACG,GCG |
T55A |
XP_011520517.1 |
XM_011522216.2 |
369 |
Intron |
|
|
XP_011520518.1 |
XM_011522217.1 |
369 |
Missense Mutation |
ACG,GCG |
T55A |
XP_011520519.1 |
XM_011522218.2 |
369 |
Missense Mutation |
ACG,GCG |
T55A |
XP_011520520.1 |
XM_017022723.1 |
369 |
Missense Mutation |
ACG,GCG |
T55A |
XP_016878212.1 |
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