Product Details

SNP ID

rs6604980

Assay Type

Functionally Tested

NCBI dbSNP Submissions

36

Location

Chr.1:1659065 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ACCTCCGGCCCAGAACTCGAGACAA[C/G]GACAGGGGCTCGCTCTGTGCGGCAC

Phenotype

MIM: 176873

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

CDK11B PubMed Links

Additional Information

For this assay, SNP(s) [rs79113395] are located under a probe 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

CDK11B

Gene Name

cyclin dependent kinase 11B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001291345.1	33	UTR 5			NP_001278274.1
NM_001787.2	33	UTR 5			NP_001778.2
NM_033486.2	33	UTR 5			NP_277021.2
NM_033487.2	33	UTR 5			NP_277022.1
NM_033489.2	33	UTR 5			NP_277024.2
NM_033490.2	33	UTR 5			NP_277025.1
XM_006711065.3	33	UTR 5			XP_006711128.1
XM_011542490.2	33	UTR 5			XP_011540792.1
XM_011542491.2	33	Intron			XP_011540793.1
XM_011542492.2	33	Intron			XP_011540794.1
XM_011542493.2	33	UTR 5			XP_011540795.1
XM_011542494.2	33	UTR 5			XP_011540796.1
XM_011542495.2	33	UTR 5			XP_011540797.1
XM_011542496.2	33	Intron			XP_011540798.1
XM_017002925.1	33	UTR 5			XP_016858414.1
XM_017002926.1	33	UTR 5			XP_016858415.1
XM_017002927.1	33	UTR 5			XP_016858416.1
XM_017002928.1	33	UTR 5			XP_016858417.1

Gene

SLC35E2B

Gene Name

solute carrier family 35 member E2B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001110781.2	33	Intron			NP_001104251.1
NM_001290264.1	33	Intron			NP_001277193.1

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