Product Details

SNP ID

rs143671992

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.3:187698925 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GAAGACGCGCATGCGCACCGAGCCC[G/T]CCCGCTGGGCGCGGTCCAGGAACAT

Phenotype

MIM: 609138

Polymorphism

G/T, Transversion Substitution

Allele Nomenclature

Literature Links

LOC100131635 PubMed Links

Additional Information

For this assay, SNP(s) [rs11707167] are located under a probe 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

LOC100131635

Gene Name

hCG1645011-like

There are no transcripts associated with this gene.

Gene

RTP2

Gene Name

receptor transporter protein 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001004312.2	825	Missense Mutation			NP_001004312.2
XM_017006301.1	825	Missense Mutation			XP_016861790.1
XM_017006302.1	825	Missense Mutation			XP_016861791.1

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