Product Details

SNP ID

rs13208685

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.6:126351935 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AAGTTTAATAACAGTATACTCCCTA[A/G]GTCAGTGGTTTTCAAGCTTTACTAA

Phenotype

MIM: 611264

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

CENPW PubMed Links

Additional Information

For this assay, SNP(s) [rs74340853] 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

CENPW

Gene Name

centromere protein W

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001012507.3		Intron			NP_001012525.1
NM_001286524.1		Intron			NP_001273453.1
NM_001286525.1		Intron			NP_001273454.1
XM_017010845.1		Intron			XP_016866334.1

View Full Product Details