Product Details

SNP ID

rs10248055

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.7:92572159 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GAAAATGTTGTTTCTTTCCAACAGA[A/G]AAATGGGCAAAGACTATGAAAAGCA

Phenotype

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

FAM133B PubMed Links

Additional Information

For this assay, SNP(s) [rs112853830] 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

FAM133B

Gene Name

family with sequence similarity 133 member B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001040057.2		Intron			NP_001035146.1
NM_001288584.1		Intron			NP_001275513.1
NM_152789.3		Intron			NP_690002.2
XM_011516004.2		Intron			XP_011514306.1
XM_011516005.2		Intron			XP_011514307.1

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