Product Details

SNP ID

rs199823309

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.12:64410052 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ACAGCGAGGATGGATGAACAGGCTC[A/T]ATTAGGGCTAAATCCAAATGCTGAT

Phenotype

MIM: 603180

Polymorphism

A/T, Transversion 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	523	Missense Mutation	CAA,CTA	Q6L	NP_009166.2
XM_017018748.1	523	Missense Mutation	CAA,CTA	Q6L	XP_016874237.1

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