Product Details

SNP ID
rs182615762
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.7:92566058 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCACTGCTTTTCTTCTTTTTTGCTC[G/T]CACCTAGAAAGTTTAAATTTTTGTG
Phenotype
Polymorphism
G/T, Transversion Substitution
Allele Nomenclature
Literature Links
FAM133B PubMed Links

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_001040057.2 815 Silent Mutation GGA,TGA G195* NP_001035146.1
NM_001288584.1 815 Silent Mutation GGA,TGA G195* NP_001275513.1
NM_152789.3 815 Intron NP_690002.2
XM_011516004.2 815 Nonsense Mutation GGA,TGA G195* XP_011514306.1
XM_011516005.2 815 Intron XP_011514307.1

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