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SNP ID

rs11263686

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.15:22802577 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTTGTTTAAGTATTGGGGTATAATT[G/A]CATAGAATAAGCTGCACAGATCTTA

Phenotype

MIM: 608145

Polymorphism

G/A, Transition substitution

Allele Nomenclature

Literature Links

NIPA1 PubMed Links

Gene Details

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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