Product Details

SNP ID

rs144227909

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.11:103909731 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCTTGAGCTGCAGATACAATCACAT[C/T]GTTCATGGTGATCCAACTGGATGTC

Phenotype

MIM: 609673

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

PDGFD PubMed Links

Additional Information

For this assay, SNP(s) [rs10791649] 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

PDGFD

Gene Name

platelet derived growth factor D

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_025208.4	1430	Missense Mutation	CAA,CGA	Q359R	NP_079484.1
NM_033135.3	1430	Missense Mutation	CAA,CGA	Q353R	NP_149126.1

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