Product Details

SNP ID
rs199728337
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:1472318 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GAAAGCCGTTTCATGTAGGGGGCCA[C/T]CTCGGCCGCGGTCAGAGGGGTGAAC
Phenotype
MIM: 611345
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
INTS1 PubMed Links

Gene Details

Gene
INTS1
Gene Name
integrator complex subunit 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001080453.2 6240 Missense Mutation ATG,GTG M2047V NP_001073922.2
XM_011515260.1 6240 Missense Mutation ATG,GTG M2047V XP_011513562.1
XM_011515262.2 6240 Intron XP_011513564.1
XM_017011959.1 6240 Missense Mutation ATG,GTG M2047V XP_016867448.1
XM_017011960.1 6240 Missense Mutation ATG,GTG M2047V XP_016867449.1

View Full Product Details