Product Details

SNP ID
rs7110778
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:64592542 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGGGGCAGATGTGGCTAGAGACCCA[C/T]TGGGCAATAGGGAGCCATGGAAGAG
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 Intron NP_001263255.1
NM_001276327.1 Intron NP_001263256.1
NM_144585.3 Intron NP_653186.2
NM_153378.2 Intron NP_700357.1
XM_006718430.3 Intron XP_006718493.1
XM_006718431.3 Intron XP_006718494.1

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