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CTTGCCCTGGGCGATCAGGTTCAGC[G/T]GCTTCTCCACTGCACTGCGGATGGT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603582 | ||||||||||||||||||||
Literature Links: |
PPM1F PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
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 |
PPM1F - protein phosphatase, Mg2+/Mn2+ dependent 1F | ||||||
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There are no transcripts associated with this gene. |
TOP3B - topoisomerase (DNA) III beta | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001282112.1 | 1953 | Missense Mutation | CAG,CCG | Q,P 567 | NP_001269041.1 | |
NM_001282113.1 | 1953 | Missense Mutation | CAG,CCG | Q,P 567 | NP_001269042.1 | |
NM_003935.4 | 1953 | Missense Mutation | CAG,CCG | Q,P 567 | NP_003926.1 | |
XM_005261811.1 | 1953 | Missense Mutation | CAG,CCG | Q,P 567 | XP_005261868.1 | |
XM_005261813.2 | 1953 | Missense Mutation | CAG,CCG | Q,P 431 | XP_005261870.1 | |
XM_006724349.1 | 1953 | Missense Mutation | CAG,CCG | Q,P 567 | XP_006724412.1 | |
XM_006724350.1 | 1953 | Missense Mutation | CAG,CCG | Q,P 567 | XP_006724413.1 | |
XM_011530482.1 | 1953 | Missense Mutation | CAG,CCG | Q,P 567 | XP_011528784.1 | |
XM_017029038.1 | 1953 | Missense Mutation | CAG,CCG | Q,P 567 | XP_016884527.1 | |
XM_017029039.1 | 1953 | Missense Mutation | CAG,CCG | Q,P 431 | XP_016884528.1 | |
XM_017029040.1 | 1953 | Missense Mutation | CAG,CCG | Q,P 431 | XP_016884529.1 | |
XM_017029041.1 | 1953 | Missense Mutation | CAG,CCG | Q,P 431 | XP_016884530.1 |