Product Details

SNP ID
rs149850611
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:9384838 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCCTGCGTGAGGCCGCGGAGCGCCA[A/G]CTCAATGAAGTAAGGACGCCCGGCT
Phenotype
MIM: 605586
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
IPO7 PubMed Links

Gene Details

Gene
IPO7
Gene Name
importin 7
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_006391.2 217 Silent Mutation CAA,CAG Q25Q NP_006382.1

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