Product Details
- SNP ID
-
rs140224531
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.17:8205227 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GGCCGCCCTCCCACCTTGACGATGC[A/G]GCGATAGGTCTCGTTGTGTGATGCA
- Phenotype
-
MIM: 604970
- Polymorphism
- A/G, Transition 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 |
963 |
Missense Mutation |
CGC,TGC |
R243C |
NP_001243763.1 |
NM_001284526.1 |
963 |
Missense Mutation |
CGC,TGC |
R285C |
NP_001271455.1 |
NM_001313950.1 |
963 |
Missense Mutation |
CGC,TGC |
R284C |
NP_001300879.1 |
NM_001313951.1 |
963 |
Intron |
|
|
NP_001300880.1 |
NM_001313952.1 |
963 |
Missense Mutation |
CGC,TGC |
R244C |
NP_001300881.1 |
NM_001313953.1 |
963 |
Missense Mutation |
CGC,TGC |
R252C |
NP_001300882.1 |
NM_001313954.1 |
963 |
Missense Mutation |
CGC,TGC |
R132C |
NP_001300883.1 |
NM_001313955.1 |
963 |
Missense Mutation |
CGC,TGC |
R116C |
NP_001300884.1 |
NM_004217.3 |
963 |
Missense Mutation |
CGC,TGC |
R284C |
NP_004208.2 |
XM_011524070.2 |
963 |
Missense Mutation |
CGC,TGC |
R252C |
XP_011522372.1 |
XM_011524072.2 |
963 |
Missense Mutation |
CGC,TGC |
R243C |
XP_011522374.1 |
XM_017025307.1 |
963 |
Missense Mutation |
CGC,TGC |
R243C |
XP_016880796.1 |
XM_017025308.1 |
963 |
Missense Mutation |
CGC,TGC |
R211C |
XP_016880797.1 |
XM_017025309.1 |
963 |
Missense Mutation |
CGC,TGC |
R132C |
XP_016880798.1 |
XM_017025310.1 |
963 |
Missense Mutation |
CGC,TGC |
R132C |
XP_016880799.1 |
XM_017025311.1 |
963 |
Missense Mutation |
CGC,TGC |
R132C |
XP_016880800.1 |
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