Product Details

SNP ID

rs193051407

Assay Type

Functionally tested

NCBI dbSNP Submissions

16

Location

Chr.1:192809084 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CGGGAGAACGATAATGCAAAGTGCT[A/G]TGTTCTTGGCTGTTCAACACGACTG

Phenotype

MIM: 600861

Polymorphism

A/G, 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	46	Missense Mutation	ATG,GTG	M5V	NP_002914.1

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