Product Details

SNP ID
rs190205938
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:61484015 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AAAACAAGTTTAAACTGTGTAGGTG[A/G]AATAGCAAGGAATGCTGGGAAACAA
Phenotype
MIM: 602559
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
XPO1 PubMed Links

Gene Details

Gene
XPO1
Gene Name
exportin 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_003400.3 3327 Missense Mutation CCA,TCA P867S NP_003391.1
XM_005264544.1 3327 Missense Mutation CCA,TCA P852S XP_005264601.1
XM_005264546.1 3327 Missense Mutation CCA,TCA P736S XP_005264603.1
XM_006712094.2 3327 Missense Mutation CCA,TCA P867S XP_006712157.1
XM_011533097.1 3327 Missense Mutation CCA,TCA P867S XP_011531399.1
XM_011533098.1 3327 Missense Mutation CCA,TCA P822S XP_011531400.1
XM_011533099.2 3327 Missense Mutation CCA,TCA P801S XP_011531401.1

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