Product Details

SNP ID

rs182282798

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.5:35001370 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GAATATCTCCTCTATCTCTACTACC[A/G]CAGCTCAGGTTCAAACAGCCTCCTT

Phenotype

MIM: 612471

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

AGXT2 PubMed Links

Additional Information

For this assay, SNP(s) [rs5867261] 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

AGXT2

Gene Name

alanine--glyoxylate aminotransferase 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001306173.1		Intron			NP_001293102.1
NM_031900.3		Intron			NP_114106.1
XM_005248337.2		Intron			XP_005248394.1
XM_005248338.2		Intron			XP_005248395.1
XM_017009748.1		Intron			XP_016865237.1

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