Product Details

SNP ID
rs148378818
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.11:64591682 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGAGCATGCTGGAGAACTTCTCGGC[C/T]GCCGTGCCCAGCCACCGCTGCTGGG
Phenotype
MIM: 607096
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
SLC22A12 PubMed Links

Gene Details

Gene
SLC22A12
Gene Name
solute carrier family 22 member 12
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001276326.1 873 Silent Mutation GCC,GCT A42A NP_001263255.1
NM_001276327.1 873 Silent Mutation GCC,GCT A42A NP_001263256.1
NM_144585.3 873 Silent Mutation GCC,GCT A42A NP_653186.2
NM_153378.2 873 UTR 5 NP_700357.1
XM_006718430.3 873 Silent Mutation GCC,GCT A42A XP_006718493.1
XM_006718431.3 873 Silent Mutation GCC,GCT A7A XP_006718494.1

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