Product Details

SNP ID
rs7141464
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.14:52434821 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GAGACTGTTCAGTTTTCTTTTTCCT[C/G]CTGCAGAGGCTACAGGATTAATTTA
Phenotype
MIM: 616179
Polymorphism
C/G, Transversion Substitution
Allele Nomenclature
Literature Links
TXNDC16 PubMed Links
Additional Information
For this assay, SNP(s) [rs78335689] 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
TXNDC16
Gene Name
thioredoxin domain containing 16
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001160047.1 Intron NP_001153519.1
NM_020784.2 Intron NP_065835.2
XM_017021505.1 Intron XP_016876994.1

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