Product Details

SNP ID

rs748708

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.17:78146714 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GAGAGGCGATGTTGTGGGGGGAGGG[A/G]CGCAAAAGAGCTTTTGTGAGTGATG

Phenotype

MIM: 605829

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

C17orf99 PubMed Links

Additional Information

For this assay, SNP(s) [rs145314766] 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

C17orf99

Gene Name

chromosome 17 open reading frame 99

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001163075.1		Intron			NP_001156547.1
XM_011524152.2		Intron			XP_011522454.1
XM_017023997.1		Intron			XP_016879486.1
XM_017023998.1		Intron			XP_016879487.1
XM_017023999.1		Intron			XP_016879488.1
XM_017024000.1		Intron			XP_016879489.1
XM_017024001.1		Intron			XP_016879490.1

Gene

TMC8

Gene Name

transmembrane channel like 8

There are no transcripts associated with this gene.

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