Product Details

SNP ID
rs14139
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:30629664 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TATGACCCATGTTCTGGTCTTGAAC[C/T]AGGTCAGAAAAACACTGTAATCTCC
Phenotype
MIM: 605600
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
IPO8 PubMed Links

Gene Details

Gene
IPO8
Gene Name
importin 8
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001190995.1 4658 UTR 3 NP_001177924.1
NM_006390.3 4658 UTR 3 NP_006381.2
XM_017018691.1 4658 UTR 3 XP_016874180.1
XM_017018692.1 4658 UTR 3 XP_016874181.1
XM_017018693.1 4658 Intron XP_016874182.1

View Full Product Details