Product Details

SNP ID
rs200000711
Assay Type
Functionally tested
NCBI dbSNP Submissions
6
Location
Chr.1:211941962 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGGTAGTTCTGGGACCAGTCTTCCA[A/T]ACTATACCATTGGCATCTTTCACAG
Phenotype
MIM: 611350
Polymorphism
A/T, Transversion substitution
Allele Nomenclature
Literature Links
INTS7 PubMed Links

Gene Details

Gene
INTS7
Gene Name
integrator complex subunit 7
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001199809.1 2932 Silent Mutation GTA,GTT V868V NP_001186738.1
NM_001199811.1 2932 Silent Mutation GTA,GTT V903V NP_001186740.1
NM_001199812.1 2932 Silent Mutation GTA,GTT V897V NP_001186741.1
NM_015434.3 2932 Silent Mutation GTA,GTT V917V NP_056249.1
XM_011509396.2 2932 Silent Mutation GTA,GTT V953V XP_011507698.1
XM_017000962.1 2932 Intron XP_016856451.1

View Full Product Details