Product Details

SNP ID: rs10075074
Assay Type: Functionally Tested
NCBI dbSNP Submissions: NA
Location: Chr.5:154888836 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: AAAACATTCTAGCTAACCAAAGTAA[G/T]TGGATTCTAAATTCTTTTTTTTTGT
Phenotype: MIM: 607005
Polymorphism: G/T, Transversion Substitution
Allele Nomenclature
Literature Links: GEMIN5 PubMed Links
Additional Information: For this assay, SNP(s) [rs138498500] are located under a primer sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001252156.1		Intron			NP_001239085.1
NM_015465.4		Intron			NP_056280.2