Product Details

SNP ID

rs143580706

Assay Type

Functionally Tested

NCBI dbSNP Submissions

4

Location

Chr.1:27005978 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGGCAGCCAGGTGGGATAGGCGTGA[C/G]CCAGGAGAGGTTGCACGGGGGTCAC

Phenotype

MIM: 616824

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

FAM46B PubMed Links

Additional Information

For this assay, SNP(s) [rs61737590] 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

FAM46B

Gene Name

family with sequence similarity 46 member B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_052943.3	1416	Missense Mutation	GCT,GGT	A415G	NP_443175.2

Gene

TRNP1

Gene Name

TMF1-regulated nuclear protein 1

There are no transcripts associated with this gene.

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