Product Details

SNP ID

rs10305852

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.4:147482505 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ATGATTCAAAGCACAGCCTGACTCA[G/T]ATTCCTGGAAATGAGCTACAGACCC

Phenotype

MIM: 131243

Polymorphism

G/T, Transversion Substitution

Allele Nomenclature

Literature Links

EDNRA PubMed Links

Additional Information

For this assay, SNP(s) [rs10305853] are located under a primer 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

EDNRA

Gene Name

endothelin receptor type A

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001166055.1		Intron			NP_001159527.1
NM_001256283.1		Intron			NP_001243212.1
NM_001957.3		Intron			NP_001948.1

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