Product Details

SNP ID

rs141527391

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.17:4900302 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ACGGCAGCGCGGGCCCAGCCCCAGA[C/T]GGCAGGGATCCGGGTGCAGCGCTGA

Phenotype

MIM: 100725 MIM: 609426

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

C17orf107 PubMed Links

Additional Information

For this assay, SNP(s) [rs79009580] 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

C17orf107

Gene Name

chromosome 17 open reading frame 107

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001145536.1	452	Silent Mutation	GAC,GAT	D114D	NP_001139008.1

Gene

CHRNE

Gene Name

cholinergic receptor nicotinic epsilon subunit

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000080.3	452	Intron			NP_000071.1
XM_017024115.1	452	Intron			XP_016879604.1

Gene

MINK1

Gene Name

misshapen like kinase 1

There are no transcripts associated with this gene.

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