Product Details

SNP ID

rs2842030

Assay Type

Validated

NCBI dbSNP Submissions

44

Location

Chr.1:163070705 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

GTACAAAAATACAAGAGTGTCAGGA[G/T]AAAGTTATGCTCTGGTAAATATTTT

Phenotype

MIM: 602516

Polymorphism

G/T, Transversion Substitution

Allele Nomenclature

Literature Links

RGS4 PubMed Links

Additional Information

For this assay, SNP(s) [rs75931331] are located under a probe and SNP(s) [rs75708071] 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

RGS4

Gene Name

regulator of G-protein signaling 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001102445.2		Intron			NP_001095915.1
NM_001113380.1		Intron			NP_001106851.1
NM_001113381.1		Intron			NP_001106852.1
NM_005613.5		Intron			NP_005604.1

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