Product Details

SNP ID

rs11635335

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.15:22787334 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTACGCTCGGTAGAGCAAGACCTGG[G/T]ATTTCCAGTCCCCCGCAGGGGCCTC

Phenotype

MIM: 608145

Polymorphism

G/T, Transversion Substitution

Allele Nomenclature

Literature Links

LOC283683 PubMed Links

Additional Information

For this assay, SNP(s) [rs112322285] 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

LOC283683

Gene Name

uncharacterized LOC283683

There are no transcripts associated with this gene.

Gene

NIPA1

Gene Name

non imprinted in Prader-Willi/Angelman syndrome 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001142275.1		Intron			NP_001135747.1
NM_144599.4		Intron			NP_653200.2

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