Product Details

SNP ID

rs138209054

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:130384483 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCTGGAGATAGTGACGATGTGACAG[C/G]AACTTTCCCTGGGCCTCTCTGGGCC

Phenotype

MIM: 300513

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

GPR119 PubMed Links

Gene Details

Gene

GPR119

Gene Name

G protein-coupled receptor 119

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_178471.2	1055	Missense Mutation	TCC,TGC	S322C	NP_848566.1

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