Product Details

SNP ID
rs138554889
Assay Type
Functionally tested
NCBI dbSNP Submissions
20
Location
Chr.1:222746656 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTGACGGAGACATCATGGAAGAATA[A/T]AGCACAGAGGAGGAGGAGGAAGAGG
Phenotype
Polymorphism
A/T, Transversion substitution
Allele Nomenclature
Literature Links
FAM177B PubMed Links

Gene Details

Gene
FAM177B
Gene Name
family with sequence similarity 177 member B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001324080.1 902 Silent Mutation TAA,TAT *37Y NP_001311009.1
NM_207468.2 902 Silent Mutation TAA,TAT *37Y NP_997351.2
XM_017001279.1 902 Nonsense Mutation TAA,TAT *37Y XP_016856768.1
XM_017001280.1 902 Nonsense Mutation TAA,TAT *37Y XP_016856769.1
XM_017001281.1 902 Nonsense Mutation TAA,TAT *37Y XP_016856770.1
XM_017001282.1 902 Nonsense Mutation TAA,TAT *37Y XP_016856771.1
XM_017001283.1 902 Nonsense Mutation TAA,TAT *48Y XP_016856772.1
XM_017001284.1 902 Nonsense Mutation TAA,TAT *48Y XP_016856773.1
XM_017001285.1 902 Nonsense Mutation TAA,TAT *48Y XP_016856774.1

View Full Product Details