Product Details

SNP ID

rs201941146

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.13:49220526 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCAACGTGGTGACCGTGATGCTGAT[C/T]GGGCGCTACCGGGACATGCGGACCA

Phenotype

MIM: 602885

Polymorphism

C/T, Transition 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	189	Silent Mutation	ATC,ATT	I63I	NP_001498.1

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