Product Details

SNP ID
rs138837940
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.8:28769906 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CAGCTCACCTTCTCCAGGGTCTGCA[C/T]GAACTGCTCCACAGGGATGGAACCG
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 1879 Missense Mutation ATG,GTG M574V NP_001138631.1
NM_001172562.1 1879 Missense Mutation ATG,GTG M571V NP_001166033.1
NM_018250.3 1879 Missense Mutation ATG,GTG M595V NP_060720.2
XM_006716356.2 1879 Missense Mutation ATG,GTG M595V XP_006716419.1
XM_006716357.3 1879 Missense Mutation ATG,GTG M595V XP_006716420.1
XM_011544573.1 1879 Missense Mutation ATG,GTG M574V XP_011542875.1
XM_011544574.1 1879 Missense Mutation ATG,GTG M571V XP_011542876.1
XM_011544575.2 1879 Missense Mutation ATG,GTG M571V XP_011542877.1
XM_011544576.1 1879 Missense Mutation ATG,GTG M550V XP_011542878.1

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