Product Details

SNP ID

rs200208332

Assay Type

Functionally tested

NCBI dbSNP Submissions

1

Location

Chr.1:192810395 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCCTTCTCCTGAGGAAGCACAGCTG[C/T]GGTCAGAAGCATTTGACGAGCTGCT

Phenotype

MIM: 600861

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

RGS2 PubMed Links

Gene Details

Gene

RGS2

Gene Name

regulator of G-protein signaling 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_002923.3	271	Missense Mutation	CGG,TGG	R80W	NP_002914.1

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