Product Details

SNP ID

rs1132916

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.6:138404560 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GACGCGGCGGCCCAAGCTGTGGAGA[C/G]GCCGGGCTGGAAGGCCCCGGAGGAC

Phenotype

MIM: 605825

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

HEBP2 PubMed Links

Additional Information

For this assay, SNP(s) [rs2274659] 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

HEBP2

Gene Name

heme binding protein 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001326380.1	335	Intron			NP_001313309.1
NM_001326381.1	335	Missense Mutation	ACG,AGG	T22R	NP_001313310.1
NM_014320.2	335	Missense Mutation	ACG,AGG	T22R	NP_055135.1
XM_017010631.1	335	Missense Mutation	ACG,AGG	T22R	XP_016866120.1

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