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CTACTGTAGCTCAGGAATAAACTGG[A/G]ACCAGTTGATGTTGTCAGGGCCCAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602341 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
FOXM1 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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FOXM1 - forkhead box M1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001243088.1 | 2550 | Missense Mutation | TCC,TTC | S,F 741 | NP_001230017.1 | |
NM_001243089.1 | 2550 | Missense Mutation | TCC,TTC | S,F 740 | NP_001230018.1 | |
NM_021953.3 | 2550 | Missense Mutation | TCC,TTC | S,F 756 | NP_068772.2 | |
NM_202002.2 | 2550 | Missense Mutation | TCC,TTC | S,F 794 | NP_973731.1 | |
NM_202003.2 | 2550 | Missense Mutation | TCC,TTC | S,F 741 | NP_973732.1 | |
XM_005253676.3 | 2550 | Missense Mutation | TCC,TTC | S,F 757 | XP_005253733.1 | |
XM_011520930.2 | 2550 | Missense Mutation | TCC,TTC | S,F 756 | XP_011519232.1 | |
XM_011520931.2 | 2550 | Missense Mutation | TCC,TTC | S,F 742 | XP_011519233.1 | |
XM_011520932.1 | 2550 | Intron | XP_011519234.1 | |||
XM_011520933.1 | 2550 | Intron | XP_011519235.1 | |||
XM_011520934.2 | 2550 | UTR 3 | XP_011519236.1 | |||
XM_011520935.1 | 2550 | Intron | XP_011519237.1 |
LOC100507424 - uncharacterized LOC100507424 | ||||||
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There are no transcripts associated with this gene. |
LOC101929469 - uncharacterized protein ENSP00000372125 | ||||||
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There are no transcripts associated with this gene. |