Product Details

SNP ID
rs150536363
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.3:186640547 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CACCCCAGCTGGCCCTCAACCCCTC[A/G]GCTCTGCTCTCCCGGGGCTGCAATG
Phenotype
MIM: 605954
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
FETUB PubMed Links
Additional Information
For this assay, SNP(s) [rs1047115] 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
FETUB
Gene Name
fetuin B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001308077.1 188 Silent Mutation TCA,TCG S29S NP_001295006.1
NM_001308079.1 188 Silent Mutation TCA,TCG S29S NP_001295008.1
NM_014375.2 188 Silent Mutation TCA,TCG S29S NP_055190.2
XM_005247351.3 188 UTR 5 XP_005247408.1
XM_011512681.2 188 Silent Mutation TCA,TCG S29S XP_011510983.1
XM_011512682.2 188 UTR 5 XP_011510984.1
XM_011512683.2 188 Intron XP_011510985.1

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