Product Details

SNP ID

rs1390186

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.12:70519416 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CCTTGATGAGGCTGTCTTTTAAGCT[C/T]AATTGAAGGTAGTAACAACAATCCT

Phenotype

MIM: 176882

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

PTPRB PubMed Links

Additional Information

For this assay, SNP(s) [rs17814277] 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

PTPRB

Gene Name

protein tyrosine phosphatase, receptor type B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
XM_006719528.1	8502	Intron			XP_006719591.1
XM_006719529.3	8502	Intron			XP_006719592.1
XM_011538614.1	8502	Intron			XP_011536916.1
XM_017019723.1	8502	UTR 3			XP_016875212.1
XM_017019724.1	8502	Intron			XP_016875213.1

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