Product Details

SNP ID

rs77550571

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.3:151199215 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCCAGAGTAAGCAGGAAATCGGCTG[G/T]AAGCAAATTAATTAAGTAGATGCTC

Phenotype

MIM: 611318

Polymorphism

G/T, Transversion Substitution

Allele Nomenclature

Literature Links

GPR171 PubMed Links

Additional Information

For this assay, SNP(s) [rs3773614] 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

GPR171

Gene Name

G protein-coupled receptor 171

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_013308.3	412	Missense Mutation	ACA,CCA	T58P	NP_037440.3
XM_005247402.3	412	Missense Mutation	ACA,CCA	T58P	XP_005247459.1
XM_005247403.3	412	Missense Mutation	ACA,CCA	T58P	XP_005247460.1
XM_017006274.1	412	Missense Mutation	ACA,CCA	T58P	XP_016861763.1

Gene

MED12L

Gene Name

mediator complex subunit 12 like

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_053002.5	412	Intron			NP_443728.3
XM_006713487.3	412	Intron			XP_006713550.1
XM_011512390.2	412	Intron			XP_011510692.1
XM_011512394.2	412	Intron			XP_011510696.1
XM_011512399.2	412	Intron			XP_011510701.1
XM_017005676.1	412	Intron			XP_016861165.1
XM_017005677.1	412	Intron			XP_016861166.1
XM_017005678.1	412	Intron			XP_016861167.1
XM_017005679.1	412	Intron			XP_016861168.1
XM_017005680.1	412	Intron			XP_016861169.1
XM_017005681.1	412	Intron			XP_016861170.1

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