Product Details

SNP ID

rs12194667

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.6:54853795 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AGAAGTGACTTTGACTTTTAAGTTT[C/T]ATTATTTAAAAAGGCATTTCATAAA

Phenotype

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

FAM83B PubMed Links

Additional Information

For this assay, SNP(s) [rs75710096] 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

FAM83B

Gene Name

family with sequence similarity 83 member B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001010872.2		Intron			NP_001010872.1
XM_006715022.3		Intron			XP_006715085.1
XM_011514394.2		Intron			XP_011512696.1
XM_011514395.2		Intron			XP_011512697.1
XM_017010478.1		Intron			XP_016865967.1

View Full Product Details