Product Details

SNP ID
rs59029020
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:100470489 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGCAAGGAGAAACCAGACTCTCACA[A/G]TGAAACATCTTCGTCCCCAGTTCCC
Phenotype
Polymorphism
A/G, 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 8 Missense Mutation ATG,GTG M1V NP_001011717.1

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