Product Details

SNP ID

rs12022842

Assay Type

Functionally Tested

NCBI dbSNP Submissions

36

Location

Chr.1:192644015 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GGAAGCCTTGGGAGTTGGTAAATTC[A/G]TTATCGGTAAGTTCTAAATGAAAAG

Phenotype

MIM: 607190

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

RGS13 PubMed Links

Additional Information

For this assay, SNP(s) [rs115844734] 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

RGS13

Gene Name

regulator of G-protein signaling 13

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_002927.4		Intron			NP_002918.1
NM_144766.2		Intron			NP_658912.1

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