Product Details

SNP ID
rs17059384
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.8:28769189 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GCCTTTAAGATTTGAAAGTCGGCAA[C/T]TGTGATATTTACATTGGATAGAAAG
Phenotype
MIM: 611352
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
INTS9 PubMed Links

Gene Details

Gene
INTS9
Gene Name
integrator complex subunit 9
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001145159.2 Intron NP_001138631.1
NM_001172562.1 Intron NP_001166033.1
NM_018250.3 Intron NP_060720.2
XM_006716356.2 Intron XP_006716419.1
XM_006716357.3 Intron XP_006716420.1
XM_011544573.1 Intron XP_011542875.1
XM_011544574.1 Intron XP_011542876.1
XM_011544575.2 Intron XP_011542877.1
XM_011544576.1 Intron XP_011542878.1

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