Product Details

SNP ID
rs189481330
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:2858928 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGCCTTTGCGGTGATTCAAGGGGGG[G/T]AGCACTTTGCAAGGGAGTGGTGCTG
Phenotype
MIM: 602341
Polymorphism
G/T, 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 2285 Missense Mutation ACC,CCC T653P NP_001230017.1
NM_001243089.1 2285 Missense Mutation ACC,CCC T652P NP_001230018.1
NM_021953.3 2285 Missense Mutation ACC,CCC T668P NP_068772.2
NM_202002.2 2285 Missense Mutation ACC,CCC T706P NP_973731.1
NM_202003.2 2285 Missense Mutation ACC,CCC T653P NP_973732.1
XM_005253676.3 2285 Missense Mutation ACC,CCC T669P XP_005253733.1
XM_011520930.2 2285 Missense Mutation ACC,CCC T668P XP_011519232.1
XM_011520931.2 2285 Missense Mutation ACC,CCC T654P XP_011519233.1
XM_011520932.1 2285 Intron XP_011519234.1
XM_011520933.1 2285 Intron XP_011519235.1
XM_011520934.2 2285 UTR 3 XP_011519236.1
XM_011520935.1 2285 Intron XP_011519237.1
Gene
LOC100507424
Gene Name
uncharacterized LOC100507424
There are no transcripts associated with this gene.

Gene
LOC101929469
Gene Name
uncharacterized protein ENSP00000372125
There are no transcripts associated with this gene.

View Full Product Details