Product Details

SNP ID

rs336362

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.4:142023948 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TAGGATAGCTAAATTCATTACATTT[C/T]TTTTTTTGCTTATATTACCTTACTA

Phenotype

MIM: 607494

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

INPP4B PubMed Links

Additional Information

For this assay, SNP(s) [rs543863678] 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

INPP4B

Gene Name

inositol polyphosphate-4-phosphatase type II B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001101669.1	8216	Intron			NP_001095139.1
NM_003866.2	8216	Intron			NP_003857.2
XM_005263323.3	8216	Intron			XP_005263380.1
XM_005263325.3	8216	Intron			XP_005263382.1
XM_011532391.2	8216	Intron			XP_011530693.1
XM_011532392.2	8216	Intron			XP_011530694.1
XM_017008794.1	8216	UTR 3			XP_016864283.1
XM_017008795.1	8216	Intron			XP_016864284.1
XM_017008796.1	8216	Intron			XP_016864285.1
XM_017008797.1	8216	Intron			XP_016864286.1
XM_017008798.1	8216	Intron			XP_016864287.1

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