Product Details

SNP ID

rs17031860

Assay Type

Functionally tested

NCBI dbSNP Submissions

30

Location

Chr.1:7962693 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ACTCTGCTTGAAAATGCTCCTAAAC[G/T]TTAAATTTTGGGGTATCTCAGGGTT

Phenotype

MIM: 602533

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

PARK7 PubMed Links

Gene Details

Gene

PARK7

Gene Name

Parkinsonism associated deglycase

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001123377.1		Intron			NP_001116849.1
NM_007262.4		Intron			NP_009193.2
XM_005263424.3		Intron			XP_005263481.1

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