Product Details

SNP ID
rs16941209
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.12:111044059 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
ACTCCATGGTAGTCTAGGAGCTTCC[A/G]TCAACCAAACAACCTTCCTCCTGTC
Phenotype
MIM: 610648
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
CUX2 PubMed Links

Gene Details

Gene
CUX2
Gene Name
cut like homeobox 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_015267.3 Intron NP_056082.2
XM_011538061.2 Intron XP_011536363.1
XM_011538063.2 Intron XP_011536365.1
XM_011538069.2 Intron XP_011536371.1
XM_011538070.2 Intron XP_011536372.1
XM_017019080.1 Intron XP_016874569.1
XM_017019081.1 Intron XP_016874570.1

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