Product Details

SNP ID
rs76847596
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:30630866 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCAGCTGATGTTCTTTCCTTCAGTT[A/G]TTGCTGGGCACAGTCCCAAAATTAA
Phenotype
MIM: 605600
Polymorphism
A/G, 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 3456 Silent Mutation AAC,AAT N831N NP_001177924.1
NM_006390.3 3456 Silent Mutation AAC,AAT N1036N NP_006381.2
XM_017018691.1 3456 Silent Mutation AAC,AAT N1019N XP_016874180.1
XM_017018692.1 3456 Silent Mutation AAC,AAT N974N XP_016874181.1
XM_017018693.1 3456 Intron XP_016874182.1

View Full Product Details