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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