Product Details

SNP ID

rs1713494

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.17:47118824 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

ACCTAAATGACTTTGAAAGTAGGTA[C/T]GAGGAAAAATAAAATAGGCCAAGCT

Phenotype

MIM: 116946

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

CDC27 PubMed Links

Additional Information

For this assay, SNP(s) [rs11570584] 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

CDC27

Gene Name

cell division cycle 27

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001114091.2	4667	Intron			NP_001107563.1
NM_001256.4	4667	Intron			NP_001247.3
NM_001293089.1	4667	Intron			NP_001280018.1
NM_001293091.1	4667	Intron			NP_001280020.1
XM_011525546.2	4667	UTR 3			XP_011523848.1
XM_011525547.2	4667	UTR 3			XP_011523849.1
XM_011525548.2	4667	UTR 3			XP_011523850.1
XM_011525549.2	4667	UTR 3			XP_011523851.1
XM_011525550.2	4667	UTR 3			XP_011523852.1
XM_017025481.1	4667	Intron			XP_016880970.1
XM_017025482.1	4667	UTR 3			XP_016880971.1
XM_017025483.1	4667	UTR 3			XP_016880972.1
XM_017025484.1	4667	UTR 3			XP_016880973.1
XM_017025485.1	4667	UTR 3			XP_016880974.1
XM_017025486.1	4667	UTR 3			XP_016880975.1
XM_017025487.1	4667	UTR 3			XP_016880976.1
XM_017025488.1	4667	UTR 3			XP_016880977.1

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