Product Details

SNP ID

rs13430695

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.2:100470833 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TGTCCTGAACATGTGTCGCTAAAAC[C/T]GAAGGGAAAGGCACTTCCTGGTGTG

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

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