Product Details

SNP ID
rs11006647
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.10:59651217 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
ACCTCACAGAGGTATTGTGAGGATT[C/T]GTGTTTATAAAGTGCTTCAGGCGCC
Phenotype
MIM: 614242
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
SLC16A9 PubMed Links

Gene Details

Gene
SLC16A9
Gene Name
solute carrier family 16 member 9
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001323977.1 3487 UTR 3 NP_001310906.1
NM_001323978.1 3487 UTR 3 NP_001310907.1
NM_001323979.1 3487 UTR 3 NP_001310908.1
NM_001323980.1 3487 UTR 3 NP_001310909.1
NM_001323981.1 3487 UTR 3 NP_001310910.1
NM_194298.2 3487 UTR 3 NP_919274.1
XM_017015883.1 3487 UTR 3 XP_016871372.1
XM_017015884.1 3487 UTR 3 XP_016871373.1

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