Product Details

SNP ID

rs2283578

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.19:710852 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGCTGTGAGCCGCCATTCGAGGACG[A/C]CTCTCTCCCCGGTTCCCGGGCTGAC

Phenotype

MIM: 608134

Polymorphism

A/C, Transversion Substitution

Allele Nomenclature

Literature Links

PALM PubMed Links

Additional Information

For this assay, SNP(s) [rs114029141,rs74537241] 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

PALM

Gene Name

paralemmin

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001040134.1		Intron			NP_001035224.1
NM_002579.2		Intron			NP_002570.2
XM_005259565.4		Intron			XP_005259622.1
XM_005259566.4		Intron			XP_005259623.1
XM_017026850.1		Intron			XP_016882339.1

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