Product Details

SNP ID
rs2548614
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.5:54518564 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCACGCGCTCCGACCTGTCCCTGGG[C/T]TCCCGCGGCGGCTCGGTCCCCCCGC
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_001102575.1 802 Silent Mutation GGC,GGT G204G NP_001096045.1
NM_001145427.1 802 Silent Mutation GGC,GGT G204G NP_001138899.1
NM_052870.2 802 Silent Mutation GGC,GGT G204G NP_443102.2
XM_017008997.1 802 Silent Mutation GGC,GGT G204G XP_016864486.1

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