Product Details

SNP ID

rs3196673

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.4:164957457 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGACAAGGACTAGAGGGTTTGGGTC[A/T]GCAGTGGGCTGGCTCCCGCTGGGCT

Phenotype

Polymorphism

A/T, Transversion Substitution

Allele Nomenclature

Literature Links

FAM218A PubMed Links

Additional Information

For this assay, SNP(s) [rs78250286] 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

FAM218A

Gene Name

family with sequence similarity 218 member A

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_153027.1	510	Silent Mutation			NP_694572.1

Gene

TRIM61

Gene Name

tripartite motif containing 61

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001012414.2	510	Intron			NP_001012414.1

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