Product Details

SNP ID

rs8056733

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.16:18999516 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CTCCTCCAAATAGAATGTAAGTTTC[A/G]TAAAAGCAGGGAAATGGTGTGTGGT

Phenotype

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

TMC7 PubMed Links

Additional Information

For this assay, SNP(s) [rs76485461] 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

TMC7

Gene Name

transmembrane channel like 7

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001160364.2		Intron			NP_001153836.1
NM_001300732.1		Intron			NP_001287661.1
NM_001324263.1		Intron			NP_001311192.1
NM_001324265.1		Intron			NP_001311194.1
NM_001324268.1		Intron			NP_001311197.1
NM_024847.4		Intron			NP_079123.3

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