Product Details
- SNP ID
-
rs149984910
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.10:35011869 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- TTACCTCTTGAATAAGGGCATTGTG[C/T]CGAAGCACTTTTCGTGCTTTCATGA
- Phenotype
-
MIM: 603135
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
CUL2
PubMed Links
Gene Details
- Gene
- CUL2
- Gene Name
- cullin 2
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_001198777.1 |
2480 |
Silent Mutation |
CGA,CGG |
R695R |
NP_001185706.1 |
| NM_001198778.1 |
2480 |
Silent Mutation |
CGA,CGG |
R714R |
NP_001185707.1 |
| NM_001198779.1 |
2480 |
Silent Mutation |
CGA,CGG |
R708R |
NP_001185708.1 |
| NM_001324375.1 |
2480 |
Silent Mutation |
CGA,CGG |
R632R |
NP_001311304.1 |
| NM_001324376.1 |
2480 |
Silent Mutation |
CGA,CGG |
R564R |
NP_001311305.1 |
| NM_003591.3 |
2480 |
Silent Mutation |
CGA,CGG |
R695R |
NP_003582.2 |
| XM_011519743.1 |
2480 |
Silent Mutation |
CGA,CGG |
R758R |
XP_011518045.1 |
| XM_011519744.1 |
2480 |
Silent Mutation |
CGA,CGG |
R758R |
XP_011518046.1 |
| XM_011519745.1 |
2480 |
Silent Mutation |
CGA,CGG |
R758R |
XP_011518047.1 |
| XM_011519747.1 |
2480 |
Silent Mutation |
CGA,CGG |
R695R |
XP_011518049.1 |
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