Product Details

SNP ID
rs199846327
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.13:49220762 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GTCGAGCGCTACCTGGCCATCTGCC[A/G]CCCGCTCCGCGCCCGCGTCTTGGTC
Phenotype
MIM: 602885
Polymorphism
A/G, 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_001507.1 425 Missense Mutation CAC,CGC H142R NP_001498.1

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