Product Details
- SNP ID
-
rs11042329
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.11:9394711 on Build GRCh38
- Set Membership
-
HapMap
- Context Sequence [VIC/FAM]
- AGGTTCTAACTTGAAATTTTACTTA[C/T]TAGCCCAATTGGAATTAAACTCCCA
- Phenotype
-
MIM: 605586
- Polymorphism
- C/T, 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 |
|
Intron |
|
|
NP_006382.1 |
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