Product Details

SNP ID
rs143619502
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.13:49220704 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCTCTACGTGGGCGAGGGCTGCACC[A/T]ACGCCACGCTGCTGCACATGACCGC
Phenotype
MIM: 602885
Polymorphism
A/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_001507.1 367 Missense Mutation AAC,TAC N123Y NP_001498.1

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