Product Details

SNP ID
rs2999472
Assay Type
Functionally Tested
NCBI dbSNP Submissions
40
Location
Chr.1:112393259 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
AAACTACTATAGTTGATGACAGAAT[A/G]AGAACTAGACTCCAGATTTTTTAAC
Phenotype
MIM: 615100
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
CTTNBP2NL PubMed Links
Additional Information
For this assay, SNP(s) [rs530981832,rs550691766] 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
CTTNBP2NL
Gene Name
CTTNBP2 N-terminal like
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_018704.2 Intron NP_061174.1
XM_011541781.2 Intron XP_011540083.1
XM_017001806.1 Intron XP_016857295.1

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