Product Details

SNP ID
rs192020949
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.5:54518798 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ACCCGTTCCAGTGCACCATCGACGA[C/T]CCCACCAAGCAGACCAAGTTCAAGG
Phenotype
Polymorphism
C/T, Transition 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 1036 Silent Mutation GAC,GAT D282D NP_001096045.1
NM_001145427.1 1036 Silent Mutation GAC,GAT D282D NP_001138899.1
NM_052870.2 1036 Silent Mutation GAC,GAT D282D NP_443102.2
XM_017008997.1 1036 Silent Mutation GAC,GAT D282D XP_016864486.1

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