Product Details

SNP ID

rs12092265

Assay Type

Functionally Tested

NCBI dbSNP Submissions

10

Location

Chr.1:156768673 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CTTTTCCTTGCCTCTGAACTCAAAA[C/G]CATCAGGCCTGGAGGAAAATGATAG

Phenotype

MIM: 179755

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

PRCC PubMed Links

Additional Information

For this assay, SNP(s) [rs76807267] 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

PRCC

Gene Name

papillary renal cell carcinoma (translocation-associated)

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_005973.4		Intron			NP_005964.3
XM_005245313.2		Intron			XP_005245370.1
XM_005245314.1		Intron			XP_005245371.1
XM_011509726.1		Intron			XP_011508028.1

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