Product Details

SNP ID

rs3735887

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.8:98193384 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GAGATTCACATGAAGCATTCACTCA[C/T]CTCCAAGCCTTTCTCTCTGGGGTTG

Phenotype

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

NIPAL2 PubMed Links

Additional Information

For this assay, SNP(s) [rs76909221] 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		Intron			NP_001308564.1
NM_001321636.1		Intron			NP_001308565.1
NM_024759.2		Intron			NP_079035.1
XM_011517302.2		Intron			XP_011515604.1

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