Product Details

SNP ID

rs12648488

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.4:76954766 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CGACGCCAATGAGTGTGAGCACATC[A/G]CTCAAGCCAAATGGCACAGGAAGTC

Phenotype

MIM: 612887

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

SEPT11 PubMed Links

Additional Information

For this assay, SNP(s) [rs77580140] are located under a probe 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

SEPT11

Gene Name

septin 11

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001306147.1		Intron			NP_001293076.1
NM_018243.3		Intron			NP_060713.1
XM_006714259.3		Intron			XP_006714322.1
XM_017008400.1		Intron			XP_016863889.1
XM_017008401.1		Intron			XP_016863890.1
XM_017008402.1		Intron			XP_016863891.1
XM_017008403.1		Intron			XP_016863892.1
XM_017008404.1		Intron			XP_016863893.1

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