Product Details

SNP ID
rs17406960
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.18:31592903 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGTCTTCTCTACACCCAGGGCACCG[G/T]TGAATCCAAGTGTCCTCTGATGGTC
Phenotype
MIM: 176300
Polymorphism
G/T, Transversion Substitution
Allele Nomenclature
Literature Links
TTR PubMed Links
Additional Information
For this assay, SNP(s) [rs1800458] are located under a probe 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
TTR
Gene Name
transthyretin
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_000371.3 213 Missense Mutation GGT,GTT G26V NP_000362.1

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