Product Details

SNP ID

rs11811007

Assay Type

Functionally Tested

NCBI dbSNP Submissions

33

Location

Chr.1:6524597 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CCTCCCACAGGCAATAATGGAGCTT[C/T]CCCAAGAGCTGGTCTGCCAGTCCTT

Phenotype

MIM: 611101

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

NOL9 PubMed Links

Additional Information

For this assay, SNP(s) [rs76388729] 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

NOL9

Gene Name

nucleolar protein 9

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_024654.4	3462	UTR 3			NP_078930.3
XM_005263493.3	3462	Intron			XP_005263550.1
XM_011542147.2	3462	Intron			XP_011540449.1
XM_017002337.1	3462	Intron			XP_016857826.1
XM_017002338.1	3462	Intron			XP_016857827.1
XM_017002339.1	3462	Intron			XP_016857828.1

Gene

PLEKHG5

Gene Name

pleckstrin homology and RhoGEF domain containing G5

There are no transcripts associated with this gene.

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