Product Details

SNP ID
rs181295064
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.9:5231713 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGGGTGGCTGCTGGAATCTGGACGT[C/T]CCAAAGGTGAGAGCCCTGGACTACC
Phenotype
MIM: 600910
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
INSL4 PubMed Links
Additional Information
For this assay, SNP(s) [rs12720] are located under a probe 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

Gene
INSL4
Gene Name
insulin like 4
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_002195.1 295 Missense Mutation CCC,TCC P64S NP_002186.1

View Full Product Details