Product Details

SNP ID

rs139237239

Assay Type

Functionally tested

NCBI dbSNP Submissions

4

Location

Chr.1:192811002 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCAGATGGTCTTGCTGCATTCAGGG[C/G]TTTTTTAAAGTCGGAATTCTGTGAA

Phenotype

MIM: 600861

Polymorphism

C/G, Transversion 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	329	Missense Mutation	GCT,GGT	A99G	NP_002914.1

View Full Product Details