Product Details

SNP ID

rs28412229

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.4:83142429 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGAGAAAATCTAAAGCTGTTTTTCA[A/T]CTTGTTAAGTGTGAGGTGCCTAAAA

Phenotype

MIM: 609825

Polymorphism

A/T, Transversion substitution

Allele Nomenclature

Literature Links

COQ2 PubMed Links

Gene Details

Gene

COQ2

Gene Name

coenzyme Q2, polyprenyltransferase

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_015697.7		Intron			NP_056512.5
XM_011531855.2		Intron			XP_011530157.1
XM_011531857.2		Intron			XP_011530159.1
XM_011531859.2		Intron			XP_011530161.1
XM_011531860.2		Intron			XP_011530162.1
XM_011531862.2		Intron			XP_011530164.1
XM_011531863.2		Intron			XP_011530165.1
XM_011531866.2		Intron			XP_011530168.1
XM_011531867.2		Intron			XP_011530169.1
XM_017008031.1		Intron			XP_016863520.1
XM_017008032.1		Intron			XP_016863521.1

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