Product Details

SNP ID

rs112815427

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.17:50516409 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AACTCCCATTGCCCCAGCAAAGTGC[C/T]ACCCAGGCCACCTTGGCAGCCTCTG

Phenotype

MIM: 609835

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

MYCBPAP PubMed Links

Additional Information

For this assay, SNP(s) [rs200018751] 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

MYCBPAP

Gene Name

MYCBP associated protein

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_032133.4		Intron			NP_115509.4
XM_005257725.3		Intron			XP_005257782.1
XM_005257726.2		Intron			XP_005257783.1
XM_011525342.1		Intron			XP_011523644.1
XM_011525343.1		Intron			XP_011523645.1
XM_017025205.1		Intron			XP_016880694.1

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