Product Details

SNP ID

rs199585067

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.6:150025409 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CACCGTCTCGCCTAGCCCGGGACCA[A/G]CCGAACAGCAGGAACAGAAGCGGGA

Phenotype

MIM: 611047

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

RAET1L PubMed Links

Additional Information

For this assay, SNP(s) [rs117766916,rs1543547] 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

RAET1L

Gene Name

retinoic acid early transcript 1L

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_130900.2		Intron			NP_570970.2
XM_011535486.2		Intron			XP_011533788.1

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