Product Details

SNP ID

rs428366

Assay Type

Functionally tested

NCBI dbSNP Submissions

46

Location

Chr.1:52690195 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AATGGGAAATCACTAACAAATAATT[C/T]TAAGTAGAAGTGGTGGCAGGGCTCA

Phenotype

MIM: 615623

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

COA7 PubMed Links

Gene Details

Gene

COA7

Gene Name

cytochrome c oxidase assembly factor 7 (putative)

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_023077.2		Intron			NP_075565.2

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