Product Details

SNP ID

rs150416503

Assay Type

Functionally tested

NCBI dbSNP Submissions

6

Location

Chr.1:43949941 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CGGTGGAATGTGGGGCTGTCTTCCC[A/G]CTGCTGGAGCAGCTGCTACAGCAGC

Phenotype

MIM: 610411

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

IPO13 PubMed Links

Gene Details

Gene

IPO13

Gene Name

importin 13

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_014652.3	1404	Silent Mutation	CCA,CCG	P203P	NP_055467.3

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