Product Details

SNP ID
rs138857972
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:12661256 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AATGGGCCAAGCAAGCTTTTTTTCC[C/T]TGGCTTCTCTGTCAAATGAGTCATA
Phenotype
MIM: 602927
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
GPR19 PubMed Links

Gene Details

Gene
GPR19
Gene Name
G protein-coupled receptor 19
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_006143.2 3891 Missense Mutation AAG,AGG K398R NP_006134.1
XM_011520623.2 3891 Missense Mutation AAG,AGG K417R XP_011518925.1
XM_011520624.2 3891 Missense Mutation AAG,AGG K417R XP_011518926.1
XM_011520625.2 3891 Missense Mutation AAG,AGG K398R XP_011518927.1
XM_017019212.1 3891 Missense Mutation AAG,AGG K417R XP_016874701.1
XM_017019213.1 3891 Missense Mutation AAG,AGG K417R XP_016874702.1
XM_017019214.1 3891 Missense Mutation AAG,AGG K417R XP_016874703.1
XM_017019215.1 3891 Missense Mutation AAG,AGG K417R XP_016874704.1
XM_017019216.1 3891 Missense Mutation AAG,AGG K398R XP_016874705.1

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