Product Details

SNP ID

rs199840661

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.8:73292259 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTTACCCTCTGATTCTGATGACAAA[C/T]GCCAATTTGGGTTCTGCAGGTACAT

Phenotype

MIM: 607599 MIM: 604166

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

C8orf89 PubMed Links

Additional Information

For this assay, SNP(s) [rs534535242,rs566736753] 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

C8orf89

Gene Name

chromosome 8 open reading frame 89

There are no transcripts associated with this gene.

Gene

RDH10

Gene Name

retinol dehydrogenase 10 (all-trans)

There are no transcripts associated with this gene.

Gene

RPL7

Gene Name

ribosomal protein L7

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000971.3	885	Intron			NP_000962.2
XM_006716463.2	885	Silent Mutation	GCA,GCG	A50A	XP_006716526.1

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