Product Details

SNP ID
rs139823239
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.X:71068256 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCGGCCCGTAAGCGTCGGTCAGGTC[C/T]TGCGGCTTCGAGTTAAGGCGCCGGG
Phenotype
MIM: 300883
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
SNX12 PubMed Links

Gene Details

Gene
SNX12
Gene Name
sorting nexin 12
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001256185.1 193 Silent Mutation CAA,CAG Q17Q NP_001243114.1
NM_001256186.1 193 Silent Mutation CAA,CAG Q17Q NP_001243115.1
NM_001256187.1 193 Silent Mutation CAA,CAG Q17Q NP_001243116.1
NM_001256188.1 193 Silent Mutation CAA,CAG Q17Q NP_001243117.1
NM_013346.3 193 Silent Mutation CAA,CAG Q17Q NP_037478.2

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