Product Details
- SNP ID
-
rs151097288
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.8:132868223 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CAGTGTGCAGAGGATGGCAGCTTCC[A/G]GTAAGGCTTATGTCAGCAGCGAACT
- Phenotype
-
MIM: 188450
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
TG
PubMed Links
Gene Details
- Gene
- TG
- Gene Name
- thyroglobulin
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_003235.4 |
234 |
Missense Mutation |
CAG,CGG |
Q59R |
NP_003226.4 |
| XM_005251038.4 |
234 |
Missense Mutation |
CAG,CGG |
Q59R |
XP_005251095.1 |
| XM_005251040.4 |
234 |
Missense Mutation |
CAG,CGG |
Q59R |
XP_005251097.1 |
| XM_005251042.4 |
234 |
Missense Mutation |
CAG,CGG |
Q59R |
XP_005251099.1 |
| XM_006716622.3 |
234 |
Missense Mutation |
CAG,CGG |
Q59R |
XP_006716685.1 |
| XM_017013793.1 |
234 |
Missense Mutation |
CAG,CGG |
Q59R |
XP_016869282.1 |
| XM_017013794.1 |
234 |
Missense Mutation |
CAG,CGG |
Q59R |
XP_016869283.1 |
| XM_017013795.1 |
234 |
Missense Mutation |
CAG,CGG |
Q59R |
XP_016869284.1 |
| XM_017013796.1 |
234 |
Missense Mutation |
CAG,CGG |
Q59R |
XP_016869285.1 |
| XM_017013797.1 |
234 |
Missense Mutation |
AGT,GGT |
S5G |
XP_016869286.1 |
| XM_017013798.1 |
234 |
Missense Mutation |
CAG,CGG |
Q59R |
XP_016869287.1 |
| XM_017013799.1 |
234 |
Missense Mutation |
CAG,CGG |
Q59R |
XP_016869288.1 |
| XM_017013800.1 |
234 |
Missense Mutation |
CAG,CGG |
Q59R |
XP_016869289.1 |
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