Product Details

SNP ID

hCV26808298

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.1:158931738 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCTCATTTCCTACATTTCTGAAGAT[C/T]TCAAGATCTGGACTACTGTTGAAGA

Phenotype

MIM: 612677

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

PYHIN1 PubMed Links

Additional Information

For this assay, SNP(s) [rs79327872] 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

PYHIN1

Gene Name

pyrin and HIN domain family member 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_152501.4	192	UTR 5			NP_689714.2
NM_198928.4	192	UTR 5			NP_945146.1
NM_198929.4	192	UTR 5			NP_945147.1
NM_198930.3	192	UTR 5			NP_945148.1

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