Product Details

SNP ID
rs140408297
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.7:101824916 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGAACTGGGAACATTCTGTGGCTCC[C/T]GTCACCATTTCTGTGTCACTCTGAA
Phenotype
MIM: 116896
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
CUX1 PubMed Links

Gene Details

Gene
CUX1
Gene Name
cut like homeobox 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001202543.1 Intron NP_001189472.1
NM_001202544.2 Intron NP_001189473.1
NM_001202545.2 Intron NP_001189474.1
NM_001202546.2 Intron NP_001189475.1
NM_001913.4 Intron NP_001904.2
NM_181500.3 Intron NP_852477.1
NM_181552.3 Intron NP_853530.2
XM_005250150.2 Intron XP_005250207.1
XM_005250151.2 Intron XP_005250208.1
XM_005250154.3 Intron XP_005250211.1
XM_006715854.2 Intron XP_006715917.1
XM_006715855.1 Intron XP_006715918.1
XM_011515823.2 Intron XP_011514125.1
XM_011515825.1 Intron XP_011514127.1
XM_017011759.1 Intron XP_016867248.1
XM_017011760.1 Intron XP_016867249.1

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