Product Details

SNP ID

rs11771811

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.7:45160775 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AGGCCGGCATGTTCTTTGTTTCCCA[A/G]TGAAACCAACCAAAATGGATTTCTA

Phenotype

MIM: 605155

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

RAMP3 PubMed Links

Additional Information

For this assay, SNP(s) [rs116428133] 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

RAMP3

Gene Name

receptor (G protein-coupled) activity modifying protein 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_005856.2		Intron			NP_005847.1
XM_006715631.3		Intron			XP_006715694.1
XM_017011666.1		Intron			XP_016867155.1

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