Product Details

SNP ID

rs76909221

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.8:98193386 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GATTCACATGAAGCATTCACTCACC[G/T]CCAAGCCTTTCTCTCTGGGGTTGTG

Phenotype

Polymorphism

G/T, Transversion Substitution

Allele Nomenclature

Literature Links

NIPAL2 PubMed Links

Additional Information

For this assay, SNP(s) [rs3735887] 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

NIPAL2

Gene Name

NIPA like domain containing 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001321635.1	1322	Intron			NP_001308564.1
NM_001321636.1	1322	Intron			NP_001308565.1
NM_024759.2	1322	Silent Mutation	AGG,CGG	R356R	NP_079035.1
XM_011517302.2	1322	Intron			XP_011515604.1

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