Product Details
- SNP ID
-
rs147771907
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
13
- Location
-
Chr.1:9037907 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CCGGGCCCCACTCACCTGGATGAAC[A/G]GGAAGATCAAGCCCACGGTGAAGTT
- Phenotype
-
MIM: 138230
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
SLC2A5
PubMed Links
Gene Details
- Gene
- SLC2A5
- Gene Name
- solute carrier family 2 member 5
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001135585.1 |
1513 |
Intron |
|
|
NP_001129057.1 |
NM_003039.2 |
1513 |
Missense Mutation |
CCG,CTG |
P431L |
NP_003030.1 |
XM_005263491.3 |
1513 |
Missense Mutation |
CCG,CTG |
P431L |
XP_005263548.1 |
XM_017002133.1 |
1513 |
Missense Mutation |
CCG,CTG |
P431L |
XP_016857622.1 |
XM_017002134.1 |
1513 |
Missense Mutation |
CCG,CTG |
P431L |
XP_016857623.1 |
XM_017002135.1 |
1513 |
Missense Mutation |
CCG,CTG |
P431L |
XP_016857624.1 |
XM_017002136.1 |
1513 |
Missense Mutation |
CCG,CTG |
P431L |
XP_016857625.1 |
XM_017002137.1 |
1513 |
Missense Mutation |
CCG,CTG |
P431L |
XP_016857626.1 |
XM_017002138.1 |
1513 |
Missense Mutation |
CCG,CTG |
P431L |
XP_016857627.1 |
XM_017002139.1 |
1513 |
Missense Mutation |
CCG,CTG |
P431L |
XP_016857628.1 |
XM_017002140.1 |
1513 |
Missense Mutation |
CCG,CTG |
P431L |
XP_016857629.1 |
XM_017002141.1 |
1513 |
Missense Mutation |
CCG,CTG |
P431L |
XP_016857630.1 |
XM_017002142.1 |
1513 |
Missense Mutation |
CCG,CTG |
P372L |
XP_016857631.1 |
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