Product Details

SNP ID
rs115647706
Assay Type
Functionally tested
NCBI dbSNP Submissions
18
Location
Chr.1:78492772 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCCATGAACAATTCCAAACAGCTAG[C/T]GTCTCCTGCAGCTGCGCTTCTTTCA
Phenotype
MIM: 600563
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
PTGFR PubMed Links

Gene Details

Gene
PTGFR
Gene Name
prostaglandin F receptor
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_000959.3 295 Missense Mutation GCG,GTG A10V NP_000950.1
NM_001039585.1 295 Missense Mutation GCG,GTG A10V NP_001034674.1
XM_017001873.1 295 Missense Mutation GCG,GTG A10V XP_016857362.1

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