Product Details

SNP ID

rs201369443

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.11:82825065 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCTCTGAGATGGTGACTGCAACCAG[A/G]GTGTCTGTGATATCCTTAGTTACTC

Phenotype

MIM: 176785

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

PRCP PubMed Links

Additional Information

For this assay, SNP(s) [rs2228312] 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

PRCP

Gene Name

prolylcarboxypeptidase

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001319214.1	1596	Silent Mutation	ACC,ACT	T339T	NP_001306143.1
NM_005040.3	1596	Silent Mutation	ACC,ACT	T444T	NP_005031.1
NM_199418.3	1596	Silent Mutation	ACC,ACT	T465T	NP_955450.2
XM_005274093.1	1596	Silent Mutation	ACC,ACT	T339T	XP_005274150.1

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