Product Details

SNP ID
rs184690191
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.16:28101629 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCTGCAGAAGATCATGGGACTTGTG[A/G]ACCAGGACCTGGAGCAGCACGTTCA
Phenotype
MIM: 608411
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
XPO6 PubMed Links

Gene Details

Gene
XPO6
Gene Name
exportin 6
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001270940.1 3138 Silent Mutation GTC,GTT V1021V NP_001257869.1
NM_015171.3 3138 Silent Mutation GTC,GTT V1035V NP_055986.1
XM_005255197.3 3138 Silent Mutation GTC,GTT V961V XP_005255254.1
XM_005255198.1 3138 Silent Mutation GTC,GTT V861V XP_005255255.1
XM_005255199.2 3138 Silent Mutation GTC,GTT V690V XP_005255256.1
XM_011545772.2 3138 Intron XP_011544074.1

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