Product Details

SNP ID

rs4344970

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.2:134934089 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AATTCCACAAATATCTATTTGTCTC[A/G]TTTTGAGAATGTTACATTTCCTTGA

Phenotype

MIM: 603862

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

CCNT2 PubMed Links

Additional Information

For this assay, SNP(s) [rs118028037] are located under a primer 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

CCNT2

Gene Name

cyclin T2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001241.3		Intron			NP_001232.1
NM_001320748.1		Intron			NP_001307677.1
NM_001320749.1		Intron			NP_001307678.1
NM_058241.2		Intron			NP_490595.1
XM_017005227.1		Intron			XP_016860716.1
XM_017005228.1		Intron			XP_016860717.1
XM_017005229.1		Intron			XP_016860718.1
XM_017005230.1		Intron			XP_016860719.1
XM_017005231.1		Intron			XP_016860720.1
XM_017005232.1		Intron			XP_016860721.1
XM_017005233.1		Intron			XP_016860722.1

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