Product Details
- SNP ID
-
rs149904176
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.17:8206499 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CTCCCAGGCCACCATACCTCAGGGA[C/G]GGCGCATGCACAGACCAGCCGAAGT
- Phenotype
-
MIM: 604970
- Polymorphism
- C/G, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
AURKB
PubMed Links
Gene Details
- Gene
- AURKB
- Gene Name
- aurora kinase B
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001256834.2 |
791 |
Silent Mutation |
CCC,CCG |
P185P |
NP_001243763.1 |
NM_001284526.1 |
791 |
Silent Mutation |
CCC,CCG |
P227P |
NP_001271455.1 |
NM_001313950.1 |
791 |
Silent Mutation |
CCC,CCG |
P226P |
NP_001300879.1 |
NM_001313951.1 |
791 |
Intron |
|
|
NP_001300880.1 |
NM_001313952.1 |
791 |
Silent Mutation |
CCC,CCG |
P186P |
NP_001300881.1 |
NM_001313953.1 |
791 |
Silent Mutation |
CCC,CCG |
P194P |
NP_001300882.1 |
NM_001313954.1 |
791 |
Silent Mutation |
CCC,CCG |
P74P |
NP_001300883.1 |
NM_001313955.1 |
791 |
Silent Mutation |
CCC,CCG |
P58P |
NP_001300884.1 |
NM_004217.3 |
791 |
Silent Mutation |
CCC,CCG |
P226P |
NP_004208.2 |
XM_011524070.2 |
791 |
Silent Mutation |
CCC,CCG |
P194P |
XP_011522372.1 |
XM_011524072.2 |
791 |
Silent Mutation |
CCC,CCG |
P185P |
XP_011522374.1 |
XM_017025307.1 |
791 |
Silent Mutation |
CCC,CCG |
P185P |
XP_016880796.1 |
XM_017025308.1 |
791 |
Silent Mutation |
CCC,CCG |
P153P |
XP_016880797.1 |
XM_017025309.1 |
791 |
Silent Mutation |
CCC,CCG |
P74P |
XP_016880798.1 |
XM_017025310.1 |
791 |
Silent Mutation |
CCC,CCG |
P74P |
XP_016880799.1 |
XM_017025311.1 |
791 |
Silent Mutation |
CCC,CCG |
P74P |
XP_016880800.1 |
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