Product Details

SNP ID
rs147434204
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.X:71068178 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCTCATAGGTGGTGAAGCGCGCGCG[C/T]CCCACGCCCACCGTCTGAGGATTAA
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_001256185.1 271 Silent Mutation GGA,GGG G43G NP_001243114.1
NM_001256186.1 271 Silent Mutation GGA,GGG G43G NP_001243115.1
NM_001256187.1 271 Silent Mutation GGA,GGG G43G NP_001243116.1
NM_001256188.1 271 Silent Mutation GGA,GGG G43G NP_001243117.1
NM_013346.3 271 Silent Mutation GGA,GGG G43G NP_037478.2

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