Product Details
- SNP ID
-
rs145383853
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.17:65640964 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- AAAATGCCTTGATTCTAGTAATTAC[C/T]TGTGATTTTAGGGAGGAAATGGTGT
- Phenotype
-
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
CEP112
PubMed Links
Gene Details
- Gene
- CEP112
- Gene Name
- centrosomal protein 112
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_001037325.2 |
3049 |
Silent Mutation |
CAA,CAG |
Q189Q |
NP_001032402.1 |
| NM_001199165.2 |
3049 |
Silent Mutation |
CAA,CAG |
Q933Q |
NP_001186094.1 |
| NM_001302891.1 |
3049 |
Silent Mutation |
CAA,CAG |
Q891Q |
NP_001289820.1 |
| XM_005257119.4 |
3049 |
Silent Mutation |
CAA,CAG |
Q934Q |
XP_005257176.1 |
| XM_005257125.3 |
3049 |
Silent Mutation |
CAA,CAG |
Q626Q |
XP_005257182.1 |
| XM_005257126.4 |
3049 |
Silent Mutation |
CAA,CAG |
Q525Q |
XP_005257183.1 |
| XM_006721740.2 |
3049 |
Silent Mutation |
CAA,CAG |
Q934Q |
XP_006721803.1 |
| XM_006721744.3 |
3049 |
Intron |
|
|
XP_006721807.1 |
| XM_011524461.2 |
3049 |
Silent Mutation |
CAA,CAG |
Q933Q |
XP_011522763.1 |
| XM_011524462.2 |
3049 |
Intron |
|
|
XP_011522764.1 |
| XM_011524463.2 |
3049 |
Intron |
|
|
XP_011522765.1 |
| XM_011524464.2 |
3049 |
Silent Mutation |
CAA,CAG |
Q863Q |
XP_011522766.1 |
| XM_011524465.2 |
3049 |
Silent Mutation |
CAA,CAG |
Q703Q |
XP_011522767.1 |
| XM_011524466.2 |
3049 |
Silent Mutation |
CAA,CAG |
Q581Q |
XP_011522768.1 |
| XM_011524467.2 |
3049 |
Silent Mutation |
CAA,CAG |
Q528Q |
XP_011522769.1 |
| XM_017024302.1 |
3049 |
Silent Mutation |
CAA,CAG |
Q891Q |
XP_016879791.1 |
| XM_017024303.1 |
3049 |
Intron |
|
|
XP_016879792.1 |
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