P54928 · IMP3_SOLLC
- ProteinInositol monophosphatase 3
- GeneIMP3
- StatusUniProtKB reviewed (Swiss-Prot)
- Amino acids268 (go to sequence)
- Protein existenceEvidence at protein level
- Annotation score4/5
Variants
Variant ID(s) | Position(s) | Change | Description | Clinical significance | Provenance | ||
---|---|---|---|---|---|---|---|
vcZ1WV6ZB | 7 | V>L | Ensembl | ||||
Consequence: missense Predictions: - SIFT: tolerated (1) Somatic: No Accession: 11:g.5242811G>C Codon: GTT/CTT Consequence type: missense Cytogenetic band: Genomic location: 11:g.5242811G>C Locations: - p.Val7Leu (EnsemblPlants:Solyc11g012410.2.1) - c.19G>C (EnsemblPlants:Solyc11g012410.2.1) Source type: large scale study Cross-references: | |||||||
vcZ1WV6ZC | 9 | Q>E | Ensembl | ||||
Consequence: missense Predictions: - SIFT: tolerated (1) Somatic: No Accession: 11:g.5242817C>G Codon: CAG/GAG Consequence type: missense Cytogenetic band: Genomic location: 11:g.5242817C>G Locations: - p.Gln9Glu (EnsemblPlants:Solyc11g012410.2.1) - c.25C>G (EnsemblPlants:Solyc11g012410.2.1) Source type: large scale study Cross-references: | |||||||
vcZ1WV6ZD | 20 | K>I | Ensembl | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.1) Somatic: No Accession: 11:g.5242851A>T Codon: AAA/ATA Consequence type: missense Cytogenetic band: Genomic location: 11:g.5242851A>T Locations: - p.Lys20Ile (EnsemblPlants:Solyc11g012410.2.1) - c.59A>T (EnsemblPlants:Solyc11g012410.2.1) Source type: large scale study Cross-references: | |||||||
vcZ1WV71L | 27 | E>D | Ensembl | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.32) Somatic: No Accession: 11:g.5243430A>T Codon: GAA/GAT Consequence type: missense Cytogenetic band: Genomic location: 11:g.5243430A>T Locations: - p.Glu27Asp (EnsemblPlants:Solyc11g012410.2.1) - c.81A>T (EnsemblPlants:Solyc11g012410.2.1) Source type: large scale study Cross-references: | |||||||
vcZ1WV71N | 40 | M>T | Ensembl | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.57) Somatic: No Accession: 11:g.5243468T>C Codon: ATG/ACG Consequence type: missense Cytogenetic band: Genomic location: 11:g.5243468T>C Locations: - p.Met40Thr (EnsemblPlants:Solyc11g012410.2.1) - c.119T>C (EnsemblPlants:Solyc11g012410.2.1) Source type: large scale study Cross-references: | |||||||
vcZ1WV753 | 85 | E>V | Ensembl | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.06) Somatic: No Accession: 11:g.5244406A>T Codon: GAA/GTA Consequence type: missense Cytogenetic band: Genomic location: 11:g.5244406A>T Locations: - p.Glu85Val (EnsemblPlants:Solyc11g012410.2.1) - c.254A>T (EnsemblPlants:Solyc11g012410.2.1) Source type: large scale study Cross-references: | |||||||
vcZ1WV774 | 134 | G>A | Ensembl | ||||
Consequence: missense Predictions: - SIFT: tolerated (1) Somatic: No Accession: 11:g.5245069G>C Codon: GGT/GCT Consequence type: missense Cytogenetic band: Genomic location: 11:g.5245069G>C Locations: - p.Gly134Ala (EnsemblPlants:Solyc11g012410.2.1) - c.401G>C (EnsemblPlants:Solyc11g012410.2.1) Source type: large scale study Cross-references: | |||||||
vcZ1WV775 | 135 | I>V | Ensembl | ||||
Consequence: missense Predictions: - SIFT: tolerated (1) Somatic: No Accession: 11:g.5245071A>G Codon: ATT/GTT Consequence type: missense Cytogenetic band: Genomic location: 11:g.5245071A>G Locations: - p.Ile135Val (EnsemblPlants:Solyc11g012410.2.1) - c.403A>G (EnsemblPlants:Solyc11g012410.2.1) Source type: large scale study Cross-references: | |||||||
vcZ1WV77H | 156 | V>M | Ensembl | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.26) Somatic: No Accession: 11:g.5245230G>A Codon: GTG/ATG Consequence type: missense Cytogenetic band: Genomic location: 11:g.5245230G>A Locations: - p.Val156Met (EnsemblPlants:Solyc11g012410.2.1) - c.466G>A (EnsemblPlants:Solyc11g012410.2.1) Source type: large scale study Cross-references: | |||||||
vcZ1WV79H | 175 | A>V | Ensembl | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.53) Somatic: No Accession: 11:g.5245918C>T Codon: GCT/GTT Consequence type: missense Cytogenetic band: Genomic location: 11:g.5245918C>T Locations: - p.Ala175Val (EnsemblPlants:Solyc11g012410.2.1) - c.524C>T (EnsemblPlants:Solyc11g012410.2.1) Source type: large scale study Cross-references: | |||||||
vcZ1WV7BQ | 245 | D>N | Ensembl | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.07) Somatic: No Accession: 11:g.5246565G>A Codon: GAC/AAC Consequence type: missense Cytogenetic band: Genomic location: 11:g.5246565G>A Locations: - p.Asp245Asn (EnsemblPlants:Solyc11g012410.2.1) - c.733G>A (EnsemblPlants:Solyc11g012410.2.1) Source type: large scale study Cross-references: | |||||||
vcZ1WV7BS | 263 | I>T | Ensembl | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.14) Somatic: No Accession: 11:g.5246620T>C Codon: ATC/ACC Consequence type: missense Cytogenetic band: Genomic location: 11:g.5246620T>C Locations: - p.Ile263Thr (EnsemblPlants:Solyc11g012410.2.1) - c.788T>C (EnsemblPlants:Solyc11g012410.2.1) Source type: large scale study Cross-references: |