Product Details

SNP ID

rs17651994

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.19:45935867 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GGAGAGGAAATACACCTCGGAGATA[A/T]GCGACACCCTGGTGTTCCAAGTAGA

Phenotype

MIM: 601991

Polymorphism

A/T, Transversion Substitution

Allele Nomenclature

Literature Links

NOVA2 PubMed Links

Additional Information

For this assay, SNP(s) [rs78558452] 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

NOVA2

Gene Name

NOVA alternative splicing regulator 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_002516.3	5523	UTR 3			NP_002507.1
XM_006723230.3	5523	Intron			XP_006723293.1
XM_017026838.1	5523	Intron			XP_016882327.1
XM_017026839.1	5523	Intron			XP_016882328.1
XM_017026840.1	5523	Intron			XP_016882329.1

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