Product Details

SNP ID

rs200256045

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.13:49220672 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGGGTGTTCGGGCCGCTGCTCTGCC[C/G]CCTGTCCCTCTACGTGGGCGAGGGC

Phenotype

MIM: 602885

Polymorphism

C/G, 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	335	Missense Mutation	CCC,CGC	P112R	NP_001498.1

View Full Product Details