Product Details

SNP ID

rs72477447

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.12:11091686 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGAGTGAAGGGTACTAAGTTTGCTA[C/G]CATGGTTACAGTCATATTTGAAAAG

Phenotype

MIM: 168730 MIM: 612668

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

PRH1 PubMed Links

Additional Information

For this assay, SNP(s) [rs144622176,rs200586631] 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	628	Intron			NP_001278243.1
NM_001291315.1	628	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	628	Intron			NP_001303822.1

Gene

TAS2R43

Gene Name

taste 2 receptor member 43

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_176884.2	628	Missense Mutation	CTA,GTA	L182V	NP_795365.2

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