Product Details

SNP ID

rs186831805

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.10:127549545 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCGCTGTCCACAATGCATGTGTTTT[C/G]GTGTTATCCAGTTCCATCTTCTAAG

Phenotype

MIM: 609513

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

NPS PubMed Links

Gene Details

Gene

NPS

Gene Name

neuropeptide S

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001030013.1	85	Missense Mutation	TCG,TGG	S22W	NP_001025184.1

View Full Product Details