Product Details

SNP ID

rs872614

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.4:89244491 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GTGAACAAAAAGGTTTCTGGTTAAC[A/C]TTGACTTATCAGGATGTTCAACTTT

Phenotype

MIM: 611241

Polymorphism

A/C, Transversion Substitution

Allele Nomenclature

Literature Links

GPRIN3 PubMed Links

Additional Information

For this assay, SNP(s) [rs112815945] 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

GPRIN3

Gene Name

GPRIN family member 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_198281.2	6139	UTR 3			NP_938022.2
XM_005262936.3	6139	UTR 3			XP_005262993.1
XM_005262937.4	6139	UTR 3			XP_005262994.1
XM_017008043.1	6139	UTR 3			XP_016863532.1
XM_017008044.1	6139	UTR 3			XP_016863533.1

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