Product Details

SNP ID

rs11042328

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:9394496 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TTCATTCATGTTTTATAGTCATCAT[G/T]CCTTGAATTACATTCTTCATTACAT

Phenotype

MIM: 605586

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

IPO7 PubMed Links

Gene Details

Gene

IPO7

Gene Name

importin 7

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_006391.2		Intron			NP_006382.1

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