Product Details

SNP ID
rs10877426
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:39757883 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
AGGCTACATATACAATAAAGAGAAG[C/G]ATTGAGGCAATTATTTTGATTAAGT
Phenotype
MIM: 611036
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
C12orf40 PubMed Links

Gene Details

Gene
C12orf40
Gene Name
chromosome 12 open reading frame 40
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001031748.3 3399 Intron NP_001026918.2
NM_001319247.1 3399 Intron NP_001306176.1
XM_005268806.3 3399 Intron XP_005268863.1
XM_011538231.2 3399 Intron XP_011536533.1
Gene
SLC2A13
Gene Name
solute carrier family 2 member 13
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_052885.3 3399 UTR 3 NP_443117.3
XM_011537847.2 3399 UTR 3 XP_011536149.1
XM_011537849.2 3399 Intron XP_011536151.1
XM_011537850.2 3399 Intron XP_011536152.1
XM_017018764.1 3399 UTR 3 XP_016874253.1
XM_017018765.1 3399 UTR 3 XP_016874254.1
XM_017018766.1 3399 UTR 3 XP_016874255.1

View Full Product Details