Product Details

SNP ID
rs78329184
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.12:11133310 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTAGAAGACACACAATGCCCCTCTT[C/G]TGAATCTATGGAGACGAAGGCTTCT
Phenotype
MIM: 168730 MIM: 613963
Polymorphism
C/G, Transversion Substitution
Allele Nomenclature
Literature Links
PRH1 PubMed Links
Additional Information
For this assay, SNP(s) [rs2600356] 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
PRH1
Gene Name
proline rich protein HaeIII subfamily 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001291314.1 935 Intron NP_001278243.1
NM_001291315.1 935 Intron NP_001278244.1
Gene
PRH1-PRR4
Gene Name
PRH1-PRR4 readthrough
There are no transcripts associated with this gene.

Gene
PRH1-TAS2R14
Gene Name
PRH1-TAS2R14 readthrough
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001316893.1 935 Intron NP_001303822.1
Gene
TAS2R30
Gene Name
taste 2 receptor member 30
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001097643.1 935 Missense Mutation ACA,AGA T312R NP_001091112.1

View Full Product Details