Product Details

SNP ID
rs150828236
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.5:54519090 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GTGCGACGTCTTCCAGCACTTCCTG[A/T]CGTGCCCCAGCAGCACCGACGAGAA
Phenotype
Polymorphism
A/T, 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 1328 Missense Mutation ACG,TCG T380S NP_001096045.1
NM_001145427.1 1328 Missense Mutation ACG,TCG T380S NP_001138899.1
NM_052870.2 1328 Missense Mutation ACG,TCG T380S NP_443102.2
XM_017008997.1 1328 Missense Mutation ACG,TCG T380S XP_016864486.1

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