Product Details

SNP ID
rs12830
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.10:35013777 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TGCTAAAGTTCATATTTAATGAAAA[C/T]GAAGATTCTGCATCAATATCTTCCT
Phenotype
MIM: 603135
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
CUL2 PubMed Links

Gene Details

Gene
CUL2
Gene Name
cullin 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001198777.1 2306 Silent Mutation TCA,TCG S637S NP_001185706.1
NM_001198778.1 2306 Silent Mutation TCA,TCG S656S NP_001185707.1
NM_001198779.1 2306 Silent Mutation TCA,TCG S650S NP_001185708.1
NM_001324375.1 2306 Silent Mutation TCA,TCG S574S NP_001311304.1
NM_001324376.1 2306 Silent Mutation TCA,TCG S506S NP_001311305.1
NM_003591.3 2306 Silent Mutation TCA,TCG S637S NP_003582.2
XM_011519743.1 2306 Silent Mutation TCA,TCG S700S XP_011518045.1
XM_011519744.1 2306 Silent Mutation TCA,TCG S700S XP_011518046.1
XM_011519745.1 2306 Silent Mutation TCA,TCG S700S XP_011518047.1
XM_011519747.1 2306 Silent Mutation TCA,TCG S637S XP_011518049.1

View Full Product Details