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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