Product Details

SNP ID
rs1528137
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.7:16091635 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TCTACCACACACAGCAGCGGGGGCA[C/T]AAAGCACAATTAAGATACGCAAATA
Phenotype
MIM: 614631
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
ISPD PubMed Links
Additional Information
For this assay, SNP(s) [rs139003391] 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
ISPD
Gene Name
isoprenoid synthase domain containing
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001101417.3 2767 UTR 3 NP_001094887.1
NM_001101426.3 2767 UTR 3 NP_001094896.1
XM_006715770.3 2767 UTR 3 XP_006715833.1
XM_011515499.2 2767 Intron XP_011513801.1
XM_011515500.2 2767 UTR 3 XP_011513802.1
XM_011515501.2 2767 Intron XP_011513803.1
XM_011515508.2 2767 UTR 3 XP_011513810.1
XM_011515509.2 2767 UTR 3 XP_011513811.1
XM_017012575.1 2767 Intron XP_016868064.1
XM_017012576.1 2767 Intron XP_016868065.1
XM_017012577.1 2767 UTR 3 XP_016868066.1
XM_017012578.1 2767 UTR 3 XP_016868067.1

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