Product Details

SNP ID

hCV27960677

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.4:3464843 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGCCTCAAGAGGGTGTGCTCCCCCG[C/G]CCGGTGAGTGCCTGAGTGGAGTGAC

Phenotype

MIM: 610285

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

DOK7 PubMed Links

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

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