Product Details

SNP ID
rs76854460
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.5:54518000 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGTACGACTTCAGGTCGGAGAACCC[A/C]GGAGAGATCTCGCTGCGAGAGCACG
Phenotype
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
SNX18 PubMed Links

Gene Details

Gene
SNX18
Gene Name
sorting nexin 18
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001102575.1 238 Silent Mutation CCA,CCC P16P NP_001096045.1
NM_001145427.1 238 Silent Mutation CCA,CCC P16P NP_001138899.1
NM_052870.2 238 Silent Mutation CCA,CCC P16P NP_443102.2
XM_017008997.1 238 Silent Mutation CCA,CCC P16P XP_016864486.1

View Full Product Details