Product Details

SNP ID
rs1801689
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.17:66214462 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TCCAATGCAGACTTACCCTTGAAGC[A/C]TTTGGGGACTTCGATAGTGCCATCT
Phenotype
MIM: 138700
Polymorphism
A/C, Transversion Substitution
Allele Nomenclature
Literature Links
APOH PubMed Links

Gene Details

Gene
APOH
Gene Name
apolipoprotein H
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_000042.2 1032 Missense Mutation NP_000033.2

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