Product Details

SNP ID
rs2241764
Assay Type
Validated
NCBI dbSNP Submissions
NA
Location
Chr.2:132417191 on Build GRCh38
Set Membership
HapMap Validated
Context Sequence [VIC/FAM]
GTGATGGGCCTTCTGGGGAACAGCG[T/C]CACCATTCGGGTCACCCAGGTGCTG
Phenotype
MIM: 602886
Polymorphism
T/C, Transition substitution
Allele Nomenclature
Literature Links
GPR39 PubMed Links

Gene Details

Gene
GPR39
Gene Name
G protein-coupled receptor 39
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001508.2 618 Missense Mutation GCC,GTC A50V NP_001499.1
XM_011511021.2 618 Missense Mutation GCC,GTC A50V XP_011509323.1

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