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GTCCAGGGTGTGGCCCAGGACCTGG[C/T]GGTAGTCGGCCTTGCCCTGGGCGAT
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 | |||
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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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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 | 1989 | Missense Mutation | CAC,CGC | H,R 579 | NP_001269041.1 | |
NM_001282113.1 | 1989 | Missense Mutation | CAC,CGC | H,R 579 | NP_001269042.1 | |
NM_003935.4 | 1989 | Missense Mutation | CAC,CGC | H,R 579 | NP_003926.1 | |
XM_005261811.1 | 1989 | Missense Mutation | CAC,CGC | H,R 579 | XP_005261868.1 | |
XM_005261813.2 | 1989 | Missense Mutation | CAC,CGC | H,R 443 | XP_005261870.1 | |
XM_006724349.1 | 1989 | Missense Mutation | CAC,CGC | H,R 579 | XP_006724412.1 | |
XM_006724350.1 | 1989 | Missense Mutation | CAC,CGC | H,R 579 | XP_006724413.1 | |
XM_011530482.1 | 1989 | Missense Mutation | CAC,CGC | H,R 579 | XP_011528784.1 | |
XM_017029038.1 | 1989 | Missense Mutation | CAC,CGC | H,R 579 | XP_016884527.1 | |
XM_017029039.1 | 1989 | Missense Mutation | CAC,CGC | H,R 443 | XP_016884528.1 | |
XM_017029040.1 | 1989 | Missense Mutation | CAC,CGC | H,R 443 | XP_016884529.1 | |
XM_017029041.1 | 1989 | Missense Mutation | CAC,CGC | H,R 443 | XP_016884530.1 |