Product Details
- SNP ID
-
rs199861756
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.13:49220446 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CCGCTGCTCGCCCTTTCCCCTGGGG[A/G]CGCTGGTGCCGGTGACCGCTGTGTG
- 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 |
109 |
Missense Mutation |
ACG,GCG |
T37A |
NP_001498.1 |
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