Product Details

SNP ID

rs2344206

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.4:3470595 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GGTGGGGCCGGCTGGCTTGTGGAAG[A/G]TGTGAGAAGCCGTCGTGGCAAATTC

Phenotype

MIM: 610285

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

DOK7 PubMed Links

Additional Information

For this assay, SNP(s) [rs74705472] 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

DOK7

Gene Name

docking protein 7

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001164673.1		Intron			NP_001158145.1
NM_001256896.1		Intron			NP_001243825.1
NM_001301071.1		Intron			NP_001288000.1
NM_173660.4		Intron			NP_775931.3
XM_011513435.2		Intron			XP_011511737.1
XM_011513437.2		Intron			XP_011511739.1
XM_017008038.1		Intron			XP_016863527.1

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