Product Details

SNP ID

rs4130761

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.4:158776458 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GACTGCCAACTCTCTCTCTGATATG[C/T]CTGGAAAATTGGACATTTTTTGTCT

Phenotype

MIM: 612768

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

FNIP2 PubMed Links

Additional Information

For this assay, SNP(s) [rs4632606] 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

FNIP2

Gene Name

folliculin interacting protein 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001323916.1		Intron			NP_001310845.1
NM_020840.2		Intron			NP_065891.1
XM_005263156.1		Intron			XP_005263213.1
XM_005263158.1		Intron			XP_005263215.1
XM_005263160.3		Intron			XP_005263217.1
XM_011532154.2		Intron			XP_011530456.1
XM_017008487.1		Intron			XP_016863976.1

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