Product Details

SNP ID

rs35719782

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.8:58009275 on Build GRCh38

Set Membership

Validated

Context Sequence [VIC/FAM]

AAGGAGTTTGCAGATGGGAGCGAAG[C/T]ACCACTGTTGATAATAACCTGAGAG

Phenotype

MIM: 611394

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

FAM110B PubMed Links

Additional Information

For this assay, SNP(s) [rs7828484] 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

FAM110B

Gene Name

family with sequence similarity 110 member B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_147189.2		Intron			NP_671722.1
XM_005251324.2		Intron			XP_005251381.1
XM_005251325.3		Intron			XP_005251382.1
XM_005251326.2		Intron			XP_005251383.1
XM_017013948.1		Intron			XP_016869437.1

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