Product Details

SNP ID
rs201181059
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:64592866 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GATTCTGGTGGGAGCTGCTGCGTGC[A/G]GCCCTGCCTCAGACAGGTGAGTACC
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 1237 Missense Mutation AGC,GGC S164G NP_001263255.1
NM_001276327.1 1237 Missense Mutation AGC,GGC S164G NP_001263256.1
NM_144585.3 1237 Missense Mutation AGC,GGC S164G NP_653186.2
NM_153378.2 1237 UTR 5 NP_700357.1
XM_006718430.3 1237 Missense Mutation AGC,GGC S164G XP_006718493.1
XM_006718431.3 1237 Missense Mutation AGC,GGC S129G XP_006718494.1

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