Product Details

SNP ID

rs11263687

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.15:22788625 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AACACCAGATGTAAGACATTAGGGA[C/A]AAACGAAGGAAAGCTGAATACCAGC

Phenotype

MIM: 608145

Polymorphism

C/A, Transversion substitution

Allele Nomenclature

Literature Links

LOC283683 PubMed Links

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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