Product Details

SNP ID
rs3825017
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:64591802 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTATTTCCATCCCGCCGGGCCCCAA[T/C]CAGAGGCCCCACCAGTGCCGCCGCT
Phenotype
MIM: 607096
Polymorphism
T/C, 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_001276326.1 993 Silent Mutation AAC,AAT N82N NP_001263255.1
NM_001276327.1 993 Silent Mutation AAC,AAT N82N NP_001263256.1
NM_144585.3 993 Silent Mutation AAC,AAT N82N NP_653186.2
NM_153378.2 993 UTR 5 NP_700357.1
XM_006718430.3 993 Silent Mutation AAC,AAT N82N XP_006718493.1
XM_006718431.3 993 Silent Mutation AAC,AAT N47N XP_006718494.1

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