Product Details

SNP ID
rs201873966
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:1473084 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CAGCCCCACTCACCCTCGCCCTCTT[C/T]GTCCAGGCCTCGGTCGGTCCTGTCG
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 6159 Missense Mutation AAA,GAA K2020E NP_001073922.2
XM_011515260.1 6159 Missense Mutation AAA,GAA K2020E XP_011513562.1
XM_011515262.2 6159 Intron XP_011513564.1
XM_017011959.1 6159 Missense Mutation AAA,GAA K2020E XP_016867448.1
XM_017011960.1 6159 Missense Mutation AAA,GAA K2020E XP_016867449.1

View Full Product Details