Product Details

SNP ID

hCV25967230

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.11:73407422 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ACTTGACAGCTGTTACCTGCCCTAG[C/T]TGACACCTGTGCTCCAGACCCAAAC

Phenotype

MIM: 616316 MIM: 611211

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

FAM168A PubMed Links

Additional Information

For this assay, SNP(s) [rs113418337] 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

FAM168A

Gene Name

family with sequence similarity 168 member A

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001286050.1		Intron			NP_001272979.1
NM_001286051.1		Intron			NP_001272980.1
NM_015159.2		Intron			NP_055974.1

Gene

RELT

Gene Name

RELT tumor necrosis factor receptor

There are no transcripts associated with this gene.

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