Product Details

SNP ID

rs146246326

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.3:195571307 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GAAAACTTAACTTCCAGCTTGGCAG[C/G]CTCTGTGAGGTTAACTGGGGTGGCT

Phenotype

MIM: 107740

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

APOD PubMed Links

Gene Details

Gene

APOD

Gene Name

apolipoprotein D

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001647.3	666	Missense Mutation	CCT,GCT	P102A	NP_001638.1

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