Product Details

SNP ID
rs117323059
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.15:22794245 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGGAGGACATTGTGCTGAGCGAAAC[C/A]AGCCAATCACAAATGACAAAGCCGG
Phenotype
MIM: 608145
Polymorphism
C/A, Transversion 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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