Product Details

SNP ID
rs141661757
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.5:54518691 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CGGCGGGGAGGCCTTCGTGCTGGGG[C/G]AGGCGTCAGGCTTCGTGAAGGACGG
Phenotype
Polymorphism
C/G, 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_001102575.1 929 Missense Mutation CAG,GAG Q247E NP_001096045.1
NM_001145427.1 929 Missense Mutation CAG,GAG Q247E NP_001138899.1
NM_052870.2 929 Missense Mutation CAG,GAG Q247E NP_443102.2
XM_017008997.1 929 Missense Mutation CAG,GAG Q247E XP_016864486.1

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