Product Details

SNP ID
rs140871791
Assay Type
Functionally tested
NCBI dbSNP Submissions
4
Location
Chr.1:153728720 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGTGGAGGAGGAGGAGCGGGAGCAG[A/G]AGCCCCAGGAGGGGGGAGGCTGCTA
Phenotype
MIM: 611347
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
INTS3 PubMed Links

Gene Details

Gene
INTS3
Gene Name
integrator complex subunit 3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001324475.1 14 Missense Mutation GAA,GGA E29G NP_001311404.1
NM_023015.4 14 Missense Mutation GAA,GGA E29G NP_075391.3
XM_005245459.2 14 Missense Mutation GAA,GGA E29G XP_005245516.1
XM_005245461.2 14 Intron XP_005245518.1
XM_006711490.3 14 UTR 5 XP_006711553.1
XM_011509906.2 14 Intron XP_011508208.1
XM_017002132.1 14 Intron XP_016857621.1

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