Product Details

SNP ID
rs7090346
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.10:89433565 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CTGTAAAGTGCTTGGAAAAGCATCA[C/T]GTACTTAGTAGTCACAACGTAAATA
Phenotype
MIM: 611910
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
SLC16A12 PubMed Links

Gene Details

Gene
SLC16A12
Gene Name
solute carrier family 16 member 12
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_213606.3 Intron NP_998771.3
XM_017016237.1 Intron XP_016871726.1
XM_017016238.1 Intron XP_016871727.1
XM_017016239.1 Intron XP_016871728.1

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