Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GAGGAGCCTTTGCGGTGATTCAAGG[C/G]GGGGAGCACTTTGCAAGGGAGTGGT
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 - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS - Not Available | African American - Not Available | YRI (Yoruba)
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SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR - Not Available | |||||
AMR - Not Available |
FOXM1 - forkhead box M1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001243088.1 | 2289 | Missense Mutation | CCC,CGC | P,R 654 | NP_001230017.1 | |
NM_001243089.1 | 2289 | Missense Mutation | CCC,CGC | P,R 653 | NP_001230018.1 | |
NM_021953.3 | 2289 | Missense Mutation | CCC,CGC | P,R 669 | NP_068772.2 | |
NM_202002.2 | 2289 | Missense Mutation | CCC,CGC | P,R 707 | NP_973731.1 | |
NM_202003.2 | 2289 | Missense Mutation | CCC,CGC | P,R 654 | NP_973732.1 | |
XM_005253676.3 | 2289 | Missense Mutation | CCC,CGC | P,R 670 | XP_005253733.1 | |
XM_011520930.2 | 2289 | Missense Mutation | CCC,CGC | P,R 669 | XP_011519232.1 | |
XM_011520931.2 | 2289 | Missense Mutation | CCC,CGC | P,R 655 | XP_011519233.1 | |
XM_011520932.1 | 2289 | Intron | XP_011519234.1 | |||
XM_011520933.1 | 2289 | Intron | XP_011519235.1 | |||
XM_011520934.2 | 2289 | UTR 3 | XP_011519236.1 | |||
XM_011520935.1 | 2289 | 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. |