Product Details

SNP ID

rs3207496

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.12:85801376 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCATGTACAAAATGTACAAGCATCA[C/T]TTACCATCTATAAAACACACACACA

Phenotype

MIM: 610383

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

RASSF9 PubMed Links

Additional Information

For this assay, SNP(s) [rs145080613] 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

RASSF9

Gene Name

Ras association domain family member 9

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_005447.3	4891	Intron			NP_005438.2
XM_011538988.2	4891	UTR 3			XP_011537290.1

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