Product Details

SNP ID

rs199613305

Assay Type

Functionally Tested

NCBI dbSNP Submissions

6

Location

Chr.1:236142738 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCCACGCTGACCCCGGCCGTGCCCC[C/T]CTACGTGAAGCTTGGCCTCACCGTC

Phenotype

MIM: 604658

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

GPR137B PubMed Links

Additional Information

For this assay, SNP(s) [rs35912664] 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

GPR137B

Gene Name

G protein-coupled receptor 137B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_003272.3	207	Missense Mutation	CCC,CTC	P39L	NP_003263.1
XM_017002209.1	207	Missense Mutation	CCC,CTC	P39L	XP_016857698.1
XM_017002210.1	207	Missense Mutation	CCC,CTC	P39L	XP_016857699.1

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