Product Details

SNP ID

rs112323495

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.5:154889331 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGCTTTAACTCTTACCTTAATGCTC[C/T]CAGGAAATTTCGCCATTCTCTGATT

Phenotype

MIM: 607005

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

GEMIN5 PubMed Links

Gene Details

Gene

GEMIN5

Gene Name

gem nuclear organelle associated protein 5

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001252156.1	4429	Missense Mutation	GAG,GGG	E1449G	NP_001239085.1
NM_015465.4	4429	Missense Mutation	GAG,GGG	E1450G	NP_056280.2

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