Product Details

SNP ID

rs4877724

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.9:82981122 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CAAAAATAAATGTTTTTAGCTTATA[C/T]AATACAATAAATAACAGCTACTTTT

Phenotype

MIM: 611344

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

RASEF PubMed Links

Additional Information

For this assay, SNP(s) [rs116715552] 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

RASEF

Gene Name

RAS and EF-hand domain containing

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_152573.3	4019	UTR 3			NP_689786.2
XM_005251730.3	4019	UTR 3			XP_005251787.1
XM_005251731.3	4019	UTR 3			XP_005251788.1

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