Product Details

SNP ID
rs151275788
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.10:89433073 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGCTCAAGGCCTTTGGTCATGTGAG[G/T]CTGTAGCCAGGCACTGCTGTAGCCA
Phenotype
MIM: 611910
Polymorphism
G/T, Transversion 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 1731 Missense Mutation AGA,AGC R514S NP_998771.3
XM_017016237.1 1731 Missense Mutation AGA,AGC R514S XP_016871726.1
XM_017016238.1 1731 Missense Mutation AGA,AGC R514S XP_016871727.1
XM_017016239.1 1731 Missense Mutation AGA,AGC R514S XP_016871728.1

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