Product Details

SNP ID
hCV32355808
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.9:133255858 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ACACGGCCTCGATGCCGTTGGCCTG[G/C]TCGACCATCATGGCCTGGTGGCAGG
Phenotype
MIM: 110300
Polymorphism
G/C, Transversion Substitution
Allele Nomenclature
Literature Links
ABO PubMed Links
Additional Information
For this assay, SNP(s) [rs8176745] are located under a primer sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene
ABO
Gene Name
ABO blood group (transferase A, alpha 1-3-N-acetylgalactosaminyltransferase; transferase B, alpha 1-3-galactosyltransferase)
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_020469.2 898 Missense Mutation GAC,GAG D291E NP_065202.2

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