Product Details

SNP ID

rs201296685

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.2:100473499 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CATTTTATTTTTTAGCAGCTGGCAT[A/G]TTGTCTGAGTCAGTGGGCACCTCTT

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	150	Missense Mutation	TAT,TGT	Y48C	NP_001011717.1

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