Product Details

SNP ID

rs7961607

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.12:12737286 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TCTGCTGGCTACAGTGGGGTAACAA[C/G]CTAGAGTTGGCCACTGACTCCACAG

Phenotype

MIM: 612456

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

APOLD1 PubMed Links

Additional Information

For this assay, SNP(s) [rs116290258] 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

APOLD1

Gene Name

apolipoprotein L domain containing 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001130415.1		Intron			NP_001123887.1
NM_030817.2		Intron			NP_110444.3

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