Product Details

SNP ID
rs72559738
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:64591607 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCGTGGGTGGCCTGGGCAGGTTCCA[A/G]GTTCTCCAGACGATGGCTCTGATGG
Phenotype
MIM: 607096
Polymorphism
A/G, 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_001276326.1 798 Silent Mutation CAA,CAG Q17Q NP_001263255.1
NM_001276327.1 798 Silent Mutation CAA,CAG Q17Q NP_001263256.1
NM_144585.3 798 Silent Mutation CAA,CAG Q17Q NP_653186.2
NM_153378.2 798 Intron NP_700357.1
XM_006718430.3 798 Silent Mutation CAA,CAG Q17Q XP_006718493.1
XM_006718431.3 798 Intron XP_006718494.1

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