Product Details

SNP ID
rs200867969
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:1472351 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCGGTCAGAGGGGTGAACAGGGAGA[C/T]GCTGACCAGGGGCAAGGAGCCGGCT
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 6207 Missense Mutation ATC,GTC I2036V NP_001073922.2
XM_011515260.1 6207 Missense Mutation ATC,GTC I2036V XP_011513562.1
XM_011515262.2 6207 Intron XP_011513564.1
XM_017011959.1 6207 Missense Mutation ATC,GTC I2036V XP_016867448.1
XM_017011960.1 6207 Missense Mutation ATC,GTC I2036V XP_016867449.1

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