Product Details

SNP ID

rs1633278

Assay Type

Validated

NCBI dbSNP Submissions

44

Location

Chr.1:158935417 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

AGATTTCAGTGGGATAAAAATGTGG[C/T]TTATAGAGAGAAATGTGGATCTGTG

Phenotype

MIM: 612677

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

PYHIN1 PubMed Links

Additional Information

For this assay, SNP(s) [rs75150453] 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

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		Intron			NP_689714.2
NM_198928.4		Intron			NP_945146.1
NM_198929.4		Intron			NP_945147.1
NM_198930.3		Intron			NP_945148.1
XM_005244930.1		Intron			XP_005244987.1
XM_011509242.2		Intron			XP_011507544.1
XM_011509243.2		Intron			XP_011507545.1
XM_017000463.1		Intron			XP_016855952.1

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