Product Details

SNP ID

rs200069228

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.22:36191177 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCGACTCAGCAGACTCGGATTTTGC[C/G]CCCTTGTGCAAGTCCAGTGAGTCTT

Phenotype

MIM: 607254

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

APOL4 PubMed Links

Additional Information

For this assay, SNP(s) [rs6000173] are located under a probe and SNP(s) [rs6000172] 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

APOL4

Gene Name

apolipoprotein L4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_030643.4	1368	Silent Mutation	GGC,GGG	G315G	NP_085146.2
NM_145660.2	1368	Silent Mutation	GGC,GGG	G318G	NP_663693.1

View Full Product Details