Product Details

SNP ID
rs148273455
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.5:54518866 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCCTACAAGCTGGTGCCCACGCACA[C/T]GCAGGTGCCGGTGCATCGGCGCTAC
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 1104 Missense Mutation ACG,ATG T305M NP_001096045.1
NM_001145427.1 1104 Missense Mutation ACG,ATG T305M NP_001138899.1
NM_052870.2 1104 Missense Mutation ACG,ATG T305M NP_443102.2
XM_017008997.1 1104 Missense Mutation ACG,ATG T305M XP_016864486.1

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