Product Details

SNP ID
rs200050409
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.15:98439679 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGCCTGGTGGCTGCCCTGCCAGCCC[A/G]GCATCCTCCTCTTCCACTCCACACT
Phenotype
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
FAM169B PubMed Links

Gene Details

Gene
FAM169B
Gene Name
family with sequence similarity 169 member B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_182562.2 781 Silent Mutation GCC,GCT A177A NP_872368.2

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