Product Details

SNP ID
rs190252104
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.8:19823925 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CACCTAGCAAACGTAGCTCTCAGAA[G/T]TACATAATAGAAGGGCTGACGGAAA
Phenotype
MIM: 611353
Polymorphism
G/T, Transversion Substitution
Allele Nomenclature
Literature Links
INTS10 PubMed Links

Gene Details

Gene
INTS10
Gene Name
integrator complex subunit 10
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_018142.2 671 Missense Mutation AAG,AAT K239N NP_060612.2
XM_005273555.3 671 Missense Mutation AAG,AAT K239N XP_005273612.1
XM_005273556.3 671 Missense Mutation AAG,AAT K239N XP_005273613.1
XM_005273557.3 671 Missense Mutation AAG,AAT K239N XP_005273614.1
XM_006716355.2 671 Missense Mutation AAG,AAT K126N XP_006716418.1
XM_017013606.1 671 Missense Mutation AAG,AAT K239N XP_016869095.1
XM_017013607.1 671 Missense Mutation AAG,AAT K239N XP_016869096.1
XM_017013608.1 671 UTR 5 XP_016869097.1
XM_017013609.1 671 UTR 5 XP_016869098.1

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