Product Details

SNP ID

rs201049857

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.10:119500156 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGAAGCTCTTTTAGCTGCAGTTTGA[G/T]CATCAGGCAAATCTTCTTCCTCTTC

Phenotype

MIM: 602856

Polymorphism

G/T, Transversion Substitution

Allele Nomenclature

Literature Links

RGS10 PubMed Links

Additional Information

For this assay, SNP(s) [rs74157681] 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

RGS10

Gene Name

regulator of G-protein signaling 10

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001005339.1	575	Missense Mutation	GAT,GCT	D168A	NP_001005339.1
NM_002925.3	575	Missense Mutation	GAT,GCT	D154A	NP_002916.1
XM_017016492.1	575	Missense Mutation	GAT,GCT	D106A	XP_016871981.1
XM_017016493.1	575	Missense Mutation	GAT,GCT	D120A	XP_016871982.1

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