Product Details

SNP ID
rs1391129
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.12:59598230 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TCTGCACTTTTGTAAGGTTGAGTAA[C/T]TGTTTAACAATCTGGGCTTTACCTT
Phenotype
MIM: 603654
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
SLC16A7 PubMed Links

Gene Details

Gene
SLC16A7
Gene Name
solute carrier family 16 member 7
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001270622.1 Intron NP_001257551.1
NM_001270623.1 Intron NP_001257552.1
NM_004731.4 Intron NP_004722.2
XM_005269231.4 Intron XP_005269288.1
XM_011538989.2 Intron XP_011537291.1
XM_011538990.2 Intron XP_011537292.1
XM_011538991.2 Intron XP_011537293.1
XM_011538992.2 Intron XP_011537294.1
XM_011538993.2 Intron XP_011537295.1
XM_011538995.2 Intron XP_011537297.1
XM_017020224.1 Intron XP_016875713.1
XM_017020225.1 Intron XP_016875714.1
XM_017020226.1 Intron XP_016875715.1
XM_017020227.1 Intron XP_016875716.1

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