Product Details

SNP ID

rs141030117

Assay Type

Functionally tested

NCBI dbSNP Submissions

19

Location

Chr.1:192809076 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGCTCCAGCGGGAGAACGATAATGC[A/G]AAGTGCTATGTTCTTGGCTGTTCAA

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	38	Missense Mutation	CAA,CGA	Q2R	NP_002914.1

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