Product Details

SNP ID: rs4910051
Assay Type: Functionally Tested
NCBI dbSNP Submissions: NA
Location: Chr.11:9397659 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: TTGGGATCTCAAGAGAGATTGTATA[C/T]GCAAAACCATGTATGTGTGCTTTGT
Phenotype: MIM: 605586
Polymorphism: C/T, Transition Substitution
Allele Nomenclature
Literature Links: IPO7 PubMed Links
Additional Information: For this assay, SNP(s) [rs77899700] 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_006391.2		Intron			NP_006382.1