Product Details

SNP ID
rs13388529
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.2:100470729 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GTTGGAACCTTTAGGAGAGGATCAA[C/G]AGAGCGAGATGCTGCAGCCTTTTAC
Phenotype
Polymorphism
C/G, Transversion Substitution
Allele Nomenclature
Literature Links
NMS PubMed Links

Gene Details

Gene
NMS
Gene Name
neuromedin S
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001011717.1 Intron NP_001011717.1

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