Product Details

SNP ID
rs114874100
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:39759935 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCAATCAAAACTAGGCTGTGGAAAG[A/G]ACCAGATTAGAAGCAGGGCAGTGAA
Phenotype
MIM: 611036
Polymorphism
A/G, Transition 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 1347 Intron NP_001026918.2
NM_001319247.1 1347 Intron NP_001306176.1
XM_005268806.3 1347 Intron XP_005268863.1
XM_011538231.2 1347 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 1347 UTR 3 NP_443117.3
XM_011537847.2 1347 UTR 3 XP_011536149.1
XM_011537849.2 1347 Intron XP_011536151.1
XM_011537850.2 1347 Intron XP_011536152.1
XM_017018764.1 1347 UTR 3 XP_016874253.1
XM_017018765.1 1347 UTR 3 XP_016874254.1
XM_017018766.1 1347 UTR 3 XP_016874255.1

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