Product Details

SNP ID
hCV25958477
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.6:132815206 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AAAAGTTCTGAATGGCATCCGTCCT[A/C]CCGGAAACCTAGGAAAAGGTATCAG
Phenotype
MIM: 603660
Polymorphism
A/C, Transversion Substitution
Allele Nomenclature
Literature Links
RPS12 PubMed Links
Additional Information
For this assay, SNP(s) [rs74627356] 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

Gene
RPS12
Gene Name
ribosomal protein S12
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001016.3 Intron NP_001007.2
Gene
SNORA33
Gene Name
small nucleolar RNA, H/ACA box 33
There are no transcripts associated with this gene.

Gene
SNORD100
Gene Name
small nucleolar RNA, C/D box 100
There are no transcripts associated with this gene.

Gene
SNORD101
Gene Name
small nucleolar RNA, C/D box 101
There are no transcripts associated with this gene.

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