Product Details

SNP ID

rs192252357

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.12:3381402 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GAATGTGTGCCAGGTTGAATGGAGT[C/G]TCTGGCTTCAGATGGATTCAAGCTG

Phenotype

MIM: 610086

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

PRMT8 PubMed Links

Additional Information

For this assay, SNP(s) [rs7964818] 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

PRMT8

Gene Name

protein arginine methyltransferase 8

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001256536.1	54	Missense Mutation	TCT,TGT	S3C	NP_001243465.1
NM_019854.4	54	Intron			NP_062828.3
XM_017019644.1	54	Intron			XP_016875133.1
XM_017019645.1	54	Intron			XP_016875134.1

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