Product Details

SNP ID

rs17060661

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.8:21930388 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CAAGGACCTGAATAGCTAGAAATGT[A/G]TGCCAATAAGGGTTATAGAGTGAGA

Phenotype

MIM: 606140

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

XPO7 PubMed Links

Gene Details

Gene

XPO7

Gene Name

exportin 7

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_015024.4		Intron			NP_055839.3
XM_017013244.1		Intron			XP_016868733.1
XM_017013245.1		Intron			XP_016868734.1
XM_017013246.1		Intron			XP_016868735.1
XM_017013247.1		Intron			XP_016868736.1

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