Product Details
- SNP ID
-
rs3184982
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.4:184694614 on Build GRCh38
- Set Membership
-
HapMap
- Context Sequence [VIC/FAM]
- CATCACCTAGCAGGCTGTCAACAGG[G/T]GCATCTGCTGATGCTGTCTGGGATA
- Phenotype
-
MIM: 611511
MIM: 615421
- Polymorphism
- G/T, Transversion Substitution
- Allele Nomenclature
-
- Literature Links
-
CENPU
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs145762735] are located under a primer sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.
Gene Details
- Gene
- CENPU
- Gene Name
- centromere protein U
- Gene
- PRIMPOL
- Gene Name
- primase and DNA directed polymerase
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_001300767.1 |
2001 |
Silent Mutation |
GGG,GGT |
G377G |
NP_001287696.1 |
| NM_001300768.1 |
2001 |
Silent Mutation |
GGG,GGT |
G505G |
NP_001287697.1 |
| NM_152683.3 |
2001 |
Silent Mutation |
GGG,GGT |
G506G |
NP_689896.1 |
| XM_011531719.1 |
2001 |
Silent Mutation |
GGG,GGT |
G519G |
XP_011530021.1 |
| XM_011531720.1 |
2001 |
Silent Mutation |
GGG,GGT |
G519G |
XP_011530022.1 |
| XM_011531721.2 |
2001 |
Silent Mutation |
GGG,GGT |
G518G |
XP_011530023.1 |
| XM_011531723.1 |
2001 |
Silent Mutation |
GGG,GGT |
G390G |
XP_011530025.1 |
| XM_011531724.2 |
2001 |
Silent Mutation |
GGG,GGT |
G344G |
XP_011530026.1 |
| XM_011531725.1 |
2001 |
Silent Mutation |
GGG,GGT |
G344G |
XP_011530027.1 |
| XM_011531726.2 |
2001 |
Silent Mutation |
GGG,GGT |
G344G |
XP_011530028.1 |
| XM_011531729.1 |
2001 |
Silent Mutation |
GGG,GGT |
G287G |
XP_011530031.1 |
| XM_011531730.2 |
2001 |
Silent Mutation |
GGG,GGT |
G287G |
XP_011530032.1 |
| XM_017007864.1 |
2001 |
Silent Mutation |
GGG,GGT |
G518G |
XP_016863353.1 |
| XM_017007865.1 |
2001 |
Silent Mutation |
GGG,GGT |
G506G |
XP_016863354.1 |
| XM_017007866.1 |
2001 |
Silent Mutation |
GGG,GGT |
G505G |
XP_016863355.1 |
| XM_017007867.1 |
2001 |
UTR 3 |
|
|
XP_016863356.1 |
| XM_017007868.1 |
2001 |
UTR 3 |
|
|
XP_016863357.1 |
| XM_017007869.1 |
2001 |
Silent Mutation |
GGG,GGT |
G435G |
XP_016863358.1 |
| XM_017007870.1 |
2001 |
Silent Mutation |
GGG,GGT |
G422G |
XP_016863359.1 |
| XM_017007871.1 |
2001 |
Silent Mutation |
GGG,GGT |
G331G |
XP_016863360.1 |
| XM_017007872.1 |
2001 |
Silent Mutation |
GGG,GGT |
G287G |
XP_016863361.1 |
| XM_017007873.1 |
2001 |
Silent Mutation |
GGG,GGT |
G274G |
XP_016863362.1 |
| XM_017007874.1 |
2001 |
Silent Mutation |
GGG,GGT |
G274G |
XP_016863363.1 |
| XM_017007875.1 |
2001 |
Silent Mutation |
GGG,GGT |
G273G |
XP_016863364.1 |
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