Product Details

SNP ID
rs3745820
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.19:45591339 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GATAGAGGTTCATCCAGGCCACCCA[A/G]CCTTCCATGGGGAACTTCTCAAAGC
Phenotype
MIM: 600551 MIM: 606580
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
GPR4 PubMed Links

Gene Details

Gene
GPR4
Gene Name
G protein-coupled receptor 4
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_005282.2 2061 Silent Mutation GGC,GGT G176G NP_005273.1
XM_017026607.1 2061 Silent Mutation GGC,GGT G176G XP_016882096.1
XM_017026608.1 2061 Silent Mutation GGC,GGT G176G XP_016882097.1
Gene
OPA3
Gene Name
optic atrophy 3 (autosomal recessive, with chorea and spastic paraplegia)
There are no transcripts associated with this gene.

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