Product Details

SNP ID
rs199620482
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.5:54518622 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCCGTCGGGGCCCAAGAGCTCGGCC[A/G]CCGTGAGCCGCAACCTCAATCGCTT
Phenotype
Polymorphism
A/G, 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_001102575.1 860 Missense Mutation ACC,GCC T224A NP_001096045.1
NM_001145427.1 860 Missense Mutation ACC,GCC T224A NP_001138899.1
NM_052870.2 860 Missense Mutation ACC,GCC T224A NP_443102.2
XM_017008997.1 860 Missense Mutation ACC,GCC T224A XP_016864486.1

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