Product Details

SNP ID

rs2421173

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.10:123136691 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CGGTGCTTCCCGGGAAAAGTGGCCT[A/C]GGGCGTGAATAGGGAGGCTTCGGAC

Phenotype

MIM: 600647 MIM: 613380

Polymorphism

A/C, Transversion Substitution

Allele Nomenclature

Literature Links

HMX2 PubMed Links

Additional Information

For this assay, SNP(s) [rs115520422] 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

HMX2

Gene Name

H6 family homeobox 2

There are no transcripts associated with this gene.

Gene

HMX3

Gene Name

H6 family homeobox 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001105574.1		Intron			NP_001099044.1

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