Product Details

SNP ID

rs9783683

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.15:42583078 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TAGGAGGATAGCGTAAGATGAAGAA[A/C]AATATGTAGTGCCCCTAATAAAGTG

Phenotype

MIM: 614642

Polymorphism

A/C, Transversion Substitution

Allele Nomenclature

Literature Links

STARD9 PubMed Links

Additional Information

For this assay, SNP(s) [rs80347429] 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

STARD9

Gene Name

StAR related lipid transfer domain containing 9

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_020759.2	255	Intron			NP_065810.2
XM_011521831.2	255	Intron			XP_011520133.1
XM_011521832.2	255	Intron			XP_011520134.1
XM_011521833.2	255	Intron			XP_011520135.1
XM_011521834.2	255	Intron			XP_011520136.1
XM_011521835.2	255	Intron			XP_011520137.1
XM_011521836.2	255	UTR 5			XP_011520138.1
XM_011521837.2	255	Intron			XP_011520139.1
XM_011521839.2	255	Intron			XP_011520141.1
XM_017022439.1	255	Intron			XP_016877928.1
XM_017022440.1	255	Intron			XP_016877929.1
XM_017022441.1	255	Intron			XP_016877930.1
XM_017022442.1	255	Intron			XP_016877931.1
XM_017022443.1	255	Intron			XP_016877932.1

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