Product Details

SNP ID

rs9568169

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.13:49220514 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TCGGGGTGAGCGGCAACGTGGTGAC[A/C]GTGATGCTGATCGGGCGCTACCGGG

Phenotype

MIM: 602885

Polymorphism

A/C, 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	177	Silent Mutation	ACA,ACC	T59T	NP_001498.1

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