Product Details

SNP ID

rs117880392

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.19:10393415 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGAAGGCTTCCAGCTCGTCGTTGAA[A/G]CCCTCCATGTACTGGCGATCGGCTG

Phenotype

MIM: 605065

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

CDC37 PubMed Links

Additional Information

For this assay, SNP(s) [rs28382792] 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

CDC37

Gene Name

cell division cycle 37

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_007065.3		Intron			NP_008996.1
XM_011527652.2		Intron			XP_011525954.1

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