Product Details

SNP ID
hCV25982197
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:2877461 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTCCTGCCGCGCTGGTCACGCCAGG[C/G]GACACGCCCCCGCTTCCCCTCAGGC
Phenotype
MIM: 602341 MIM: 614085
Polymorphism
C/G, Transversion 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
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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