Product Details

SNP ID
rs2788138
Assay Type
Functionally Tested
NCBI dbSNP Submissions
28
Location
Chr.1:211942670 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TACTCCTTTAACAAATTAACTGAAC[A/C]ATTTGTACATTGCTCATTTAATAAG
Phenotype
MIM: 611350
Polymorphism
A/C, Transversion Substitution
Allele Nomenclature
Literature Links
INTS7 PubMed Links
Additional Information
For this assay, SNP(s) [rs116680092] 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
INTS7
Gene Name
integrator complex subunit 7
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001199809.1 Intron NP_001186738.1
NM_001199811.1 Intron NP_001186740.1
NM_001199812.1 Intron NP_001186741.1
NM_015434.3 Intron NP_056249.1
XM_011509396.2 Intron XP_011507698.1
XM_017000962.1 Intron XP_016856451.1

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