Product Details

SNP ID
rs116764744
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.2:100471486 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCCCGATTCTATTTAACTACTTCAA[C/T]GACCCCAACTCACTGCCAGCTATGA
Phenotype
Polymorphism
C/T, Transition 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

View Full Product Details