Product Details

SNP ID
rs150255616
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:64414909 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTTTTTGTTTTGCAATCTTATAGGC[C/T]CTGGCCTATTTTGAGCAGTTAAAAA
Phenotype
MIM: 603180
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
XPOT PubMed Links

Gene Details

Gene
XPOT
Gene Name
exportin for tRNA
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_007235.4 569 Silent Mutation GCC,GCT A21A NP_009166.2
XM_017018748.1 569 Silent Mutation GCC,GCT A21A XP_016874237.1

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