Product Details

SNP ID
rs3802948
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:64591685 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCATGCTGGAGAACTTCTCGGCCGC[C/T]GTGCCCAGCCACCGCTGCTGGGCAC
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_001276326.1 876 Silent Mutation GCC,GCT A43A NP_001263255.1
NM_001276327.1 876 Silent Mutation GCC,GCT A43A NP_001263256.1
NM_144585.3 876 Silent Mutation GCC,GCT A43A NP_653186.2
NM_153378.2 876 UTR 5 NP_700357.1
XM_006718430.3 876 Silent Mutation GCC,GCT A43A XP_006718493.1
XM_006718431.3 876 Silent Mutation GCC,GCT A8A XP_006718494.1

View Full Product Details