Product Details

SNP ID

rs1059476

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:8205013 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TTTGGAGATGAGGTCCTGGGCTCCC[A/G]TGGGCACGGAAGCGGGGAACTTTAG

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	1006	Missense Mutation	ACG,ATG	T257M	NP_001243763.1
NM_001284526.1	1006	Missense Mutation	ACG,ATG	T299M	NP_001271455.1
NM_001313950.1	1006	Missense Mutation	ACG,ATG	T298M	NP_001300879.1
NM_001313951.1	1006	Intron			NP_001300880.1
NM_001313952.1	1006	Missense Mutation	ACG,ATG	T258M	NP_001300881.1
NM_001313953.1	1006	Missense Mutation	ACG,ATG	T266M	NP_001300882.1
NM_001313954.1	1006	Missense Mutation	ACG,ATG	T146M	NP_001300883.1
NM_001313955.1	1006	Missense Mutation	ACG,ATG	T130M	NP_001300884.1
NM_004217.3	1006	Missense Mutation	ACG,ATG	T298M	NP_004208.2
XM_011524070.2	1006	Missense Mutation	ACG,ATG	T266M	XP_011522372.1
XM_011524072.2	1006	Missense Mutation	ACG,ATG	T257M	XP_011522374.1
XM_017025307.1	1006	Missense Mutation	ACG,ATG	T257M	XP_016880796.1
XM_017025308.1	1006	Missense Mutation	ACG,ATG	T225M	XP_016880797.1
XM_017025309.1	1006	Missense Mutation	ACG,ATG	T146M	XP_016880798.1
XM_017025310.1	1006	Missense Mutation	ACG,ATG	T146M	XP_016880799.1
XM_017025311.1	1006	Missense Mutation	ACG,ATG	T146M	XP_016880800.1

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