Product Details

SNP ID

rs200039762

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.16:2020581 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCCAGCGGTGGACCCCGCAGCAAAC[C/T]GCCTTGGCCTGCCCTGCCTGGCCCC

Phenotype

MIM: 607997 MIM: 606553

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

NPW PubMed Links

Gene Details

Gene

NPW

Gene Name

neuropeptide W

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001099456.2	842	Missense Mutation	CGC,TGC	R154C	NP_001092926.2

Gene

SLC9A3R2

Gene Name

SLC9A3 regulator 2

There are no transcripts associated with this gene.

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