Product Details

SNP ID

rs753027120

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.17:65641181 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATGAAAGGTTTGTTACACGCGGTCA[A/G]AAACCAGACAATAAAGATGAAATAA

Phenotype

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

CEP112 PubMed Links

Additional Information

For this assay, SNP(s) [rs75578796] 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

CEP112

Gene Name

centrosomal protein 112

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001037325.2		Intron			NP_001032402.1
NM_001199165.2		Intron			NP_001186094.1
NM_001302891.1		Intron			NP_001289820.1
XM_005257119.4		Intron			XP_005257176.1
XM_005257125.3		Intron			XP_005257182.1
XM_005257126.4		Intron			XP_005257183.1
XM_006721740.2		Intron			XP_006721803.1
XM_006721744.3		Intron			XP_006721807.1
XM_011524461.2		Intron			XP_011522763.1
XM_011524462.2		Intron			XP_011522764.1
XM_011524463.2		Intron			XP_011522765.1
XM_011524464.2		Intron			XP_011522766.1
XM_011524465.2		Intron			XP_011522767.1
XM_011524466.2		Intron			XP_011522768.1
XM_011524467.2		Intron			XP_011522769.1
XM_017024302.1		Intron			XP_016879791.1
XM_017024303.1		Intron			XP_016879792.1

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