Product Details

SNP ID

rs199619980

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:9403297 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GACTTTTTTTCTTTGTAGGCACACA[A/G]GTCTCTGAATTTTGTCTCAACACTG

Phenotype

MIM: 605586

Polymorphism

A/G, Transition 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	234	Missense Mutation	AAG,AGG	K31R	NP_006382.1

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