Product Details

SNP ID
rs142329889
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.10:89436219 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TAGCCAAAGGTACAAGAGAAAGGCA[C/T]GAGCAGAGGGAGACTTTGAAGCATT
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 1318 Missense Mutation NP_998771.3
XM_017016237.1 1318 Missense Mutation XP_016871726.1
XM_017016238.1 1318 Missense Mutation XP_016871727.1
XM_017016239.1 1318 Missense Mutation XP_016871728.1

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