Product Details

SNP ID

rs140108338

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.12:6201361 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TATCTGCGCCTCTAGTGGGATGAGT[C/T]CTGTGTGTGCATTTCCGGGAGAGAT

Phenotype

MIM: 143030

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

CD9 PubMed Links

Additional Information

For this assay, SNP(s) [rs36107890] 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

CD9

Gene Name

CD9 molecule

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001769.3		Intron			NP_001760.1
XM_005253814.3		Intron			XP_005253871.1
XM_011521040.1		Intron			XP_011519342.1

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