Product Details

SNP ID

rs141183673

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.19:12701385 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AAGCCGCCAGCCTCTCCTTGAGCAG[C/T]GGCGGGAATTGCTCAGAGAACTGCT

Phenotype

MIM: 609074 MIM: 603002

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

FBXW9 PubMed Links

Additional Information

For this assay, SNP(s) [rs16978628] 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

FBXW9

Gene Name

F-box and WD repeat domain containing 9

There are no transcripts associated with this gene.

Gene

SNORD135

Gene Name

small nucleolar RNA, C/D box 135

There are no transcripts associated with this gene.

Gene

SNORD41

Gene Name

small nucleolar RNA, C/D box 41

There are no transcripts associated with this gene.

Gene

TNPO2

Gene Name

transportin 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001136195.1	2796	Silent Mutation	CCA,CCG	P875P	NP_001129667.1
NM_001136196.1	2796	Silent Mutation	CCA,CCG	P885P	NP_001129668.1
NM_013433.4	2796	Silent Mutation	CCA,CCG	P875P	NP_038461.2

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