Product Details

SNP ID
rs141952918
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.3:184036045 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCCAGATGAATGCGGAGGCATCAAG[A/G]AGTCCGGCATGGCAACTGAGAACCT
Phenotype
MIM: 610122
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
HTR3D PubMed Links

Gene Details

Gene
HTR3D
Gene Name
5-hydroxytryptamine receptor 3D
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001145143.1 325 Missense Mutation AAG,GAG K48E NP_001138615.1
NM_001163646.1 325 Missense Mutation AAG,GAG K109E NP_001157118.1
NM_182537.2 325 Intron NP_872343.2
XM_017005854.1 325 Intron XP_016861343.1

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