Product Details

SNP ID

rs142013001

Assay Type

Functionally Tested

NCBI dbSNP Submissions

16

Location

Chr.1:78493177 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTCACAAAACCAATATTTCATTCTA[C/T]GAAAATTACATCCAAACATGTGAAA

Phenotype

MIM: 600563

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

PTGFR PubMed Links

Additional Information

For this assay, SNP(s) [rs12088246] are located under a probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

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	700	Missense Mutation	ACG,ATG	T145M	NP_000950.1
NM_001039585.1	700	Missense Mutation	ACG,ATG	T145M	NP_001034674.1
XM_017001873.1	700	Missense Mutation	ACG,ATG	T145M	XP_016857362.1

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