Product Details

SNP ID

rs426873

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.5:35052361 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGAAAAGCCATGTGAACATATCAAT[A/G]GATGTAGAAAAAAATTTGAGAAGTT

Phenotype

MIM: 612471 MIM: 176761

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

AGXT2 PubMed Links

Additional Information

For this assay, SNP(s) [rs115565909] 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

AGXT2

Gene Name

alanine--glyoxylate aminotransferase 2

There are no transcripts associated with this gene.

Gene

PRLR

Gene Name

prolactin receptor

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000949.6		Intron			NP_000940.1
NM_001204314.2		Intron			NP_001191243.1
NM_001204315.1		Intron			NP_001191244.1
NM_001204316.1		Intron			NP_001191245.1
NM_001204317.1		Intron			NP_001191246.1
NM_001204318.1		Intron			NP_001191247.1
XM_006714484.2		Intron			XP_006714547.1
XM_011514068.2		Intron			XP_011512370.1
XM_011514069.2		Intron			XP_011512371.1
XM_017009645.1		Intron			XP_016865134.1
XM_017009646.1		Intron			XP_016865135.1

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