Product Details

SNP ID
rs200097061
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.2:61485926 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ACATTTCTCTGATAATCAATGAGAA[C/T]TGCATCCAACAGAGGGGGAACAAAA
Phenotype
MIM: 602559
Polymorphism
C/T, 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 3078 Missense Mutation ATT,GTT I784V NP_003391.1
XM_005264544.1 3078 Missense Mutation ATT,GTT I769V XP_005264601.1
XM_005264546.1 3078 Missense Mutation ATT,GTT I653V XP_005264603.1
XM_006712094.2 3078 Missense Mutation ATT,GTT I784V XP_006712157.1
XM_011533097.1 3078 Missense Mutation ATT,GTT I784V XP_011531399.1
XM_011533098.1 3078 Missense Mutation ATT,GTT I739V XP_011531400.1
XM_011533099.2 3078 Missense Mutation ATT,GTT I718V XP_011531401.1

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