Product Details

SNP ID
hCV25613689
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.1:96723538 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGTGATTAGAAGAATAACAGGAGGT[G/T]GAAACTACTTATTTTTTCTTTGCAG
Phenotype
MIM: 608449
Polymorphism
G/T, Transversion Substitution
Allele Nomenclature
Literature Links
PTBP2 PubMed Links
Additional Information
For this assay, SNP(s) [rs571221800] 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
PTBP2
Gene Name
polypyrimidine tract binding protein 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001300985.1 Intron NP_001287914.1
NM_001300986.1 Intron NP_001287915.1
NM_001300987.1 Intron NP_001287916.1
NM_001300988.1 Intron NP_001287917.1
NM_001300989.1 Intron NP_001287918.1
NM_001300990.1 Intron NP_001287919.1
NM_021190.3 Intron NP_067013.1

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