Product Details

SNP ID

rs2795055

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.9:109783017 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

TCTCTGGAGATGTGAGGGAAGAAGA[C/G]AATAGGTCCTCACATCTTCACTTAC

Phenotype

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

PALM2 PubMed Links

Additional Information

For this assay, SNP(s) [rs200689137] 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

PALM2

Gene Name

paralemmin 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001037293.2		Intron			NP_001032370.1
NM_053016.5		Intron			NP_443749.5

Gene

PALM2-AKAP2

Gene Name

PALM2-AKAP2 readthrough

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_007203.4		Intron			NP_009134.1
NM_147150.2		Intron			NP_671492.1

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