Product Details

SNP ID

rs140892141

Assay Type

Functionally tested

NCBI dbSNP Submissions

2

Location

Chr.1:78492784 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCCAAACAGCTAGTGTCTCCTGCAG[C/G]TGCGCTTCTTTCAAACACAACCTGC

Phenotype

MIM: 600563

Polymorphism

C/G, Transversion 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	307	Missense Mutation	GCT,GGT	A14G	NP_000950.1
NM_001039585.1	307	Missense Mutation	GCT,GGT	A14G	NP_001034674.1
XM_017001873.1	307	Missense Mutation	GCT,GGT	A14G	XP_016857362.1

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