Product Details

SNP ID
rs199943015
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.13:49220529 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ACGTGGTGACCGTGATGCTGATCGG[G/T]CGCTACCGGGACATGCGGACCACCA
Phenotype
MIM: 602885
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
MLNR PubMed Links

Gene Details

Gene
MLNR
Gene Name
motilin receptor
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001507.1 192 Silent Mutation GGG,GGT G64G NP_001498.1

View Full Product Details