Product Details

SNP ID

rs12809349

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.12:50330661 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GGAATATCTGGGTACCCACCCAGCT[C/G]GGCCCAGAGTGAATGCATAGATGTC

Phenotype

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

FAM186A PubMed Links

Additional Information

For this assay, SNP(s) [rs80144666] are located under a probe 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

FAM186A

Gene Name

family with sequence similarity 186 member A

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001145475.1	7083	Missense Mutation	CAG,GAG	Q2316E	NP_001138947.1
XM_006719231.3	7083	Missense Mutation	CAG,GAG	Q2316E	XP_006719294.1
XM_011537890.2	7083	Missense Mutation	CAG,GAG	Q2312E	XP_011536192.1
XM_011537892.1	7083	Missense Mutation	CAG,GAG	Q2173E	XP_011536194.1

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