Product Details

SNP ID
rs28990686
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:2876908 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGCCAGGCCTGGGACTCCATTGCTG[C/T]ATCCCGCTCACCTCCAGACTGCAGT
Phenotype
MIM: 602341 MIM: 614085
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
FOXM1 PubMed Links

Gene Details

Gene
FOXM1
Gene Name
forkhead box M1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001243088.1 Intron NP_001230017.1
NM_001243089.1 Intron NP_001230018.1
NM_021953.3 Intron NP_068772.2
NM_202002.2 Intron NP_973731.1
NM_202003.2 Intron NP_973732.1
XM_005253676.3 Intron XP_005253733.1
XM_011520930.2 Intron XP_011519232.1
XM_011520931.2 Intron XP_011519233.1
XM_011520932.1 Intron XP_011519234.1
XM_011520933.1 Intron XP_011519235.1
XM_011520934.2 Intron XP_011519236.1
XM_011520935.1 Intron XP_011519237.1
Gene
RHNO1
Gene Name
RAD9-HUS1-RAD1 interacting nuclear orphan 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001252499.2 Intron NP_001239428.1
NM_001252500.2 Intron NP_001239429.1
NM_001257097.1 Intron NP_001244026.1
NM_001257098.1 Intron NP_001244027.1

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