Q9S7B2 · RS2_MAIZE
- ProteinProtein rough sheath 2
- GeneRS2
- StatusUniProtKB reviewed (Swiss-Prot)
- Organism
- Amino acids370 (go to sequence)
- Protein existenceEvidence at protein level
- Annotation score5/5
Variants
Variant ID(s) | Position(s) | Change | Description | Clinical significance | Provenance | ||
---|---|---|---|---|---|---|---|
S1_154953992 | 74 | Q>E | EnsemblPlants | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 1:g.158673585G>C Codon: CAG/GAG Consequence type: missense Cytogenetic band: Genomic location: 1:g.158673585G>C Locations: - p.Gln74Glu (EnsemblPlants:Zm00001eb029300_T001) - c.220C>G (EnsemblPlants:Zm00001eb029300_T001) - p.Gln74Glu (EnsemblPlants:Zm00001eb029300_T002) - c.220C>G (EnsemblPlants:Zm00001eb029300_T002) Source type: large scale study Cross-references: | |||||||
S1_154953897 | 105 | E>D | EnsemblPlants | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.05) Somatic: No Accession: 1:g.158673490C>G Codon: GAG/GAC Consequence type: missense Cytogenetic band: Genomic location: 1:g.158673490C>G Locations: - p.Glu105Asp (EnsemblPlants:Zm00001eb029300_T002) - c.315G>C (EnsemblPlants:Zm00001eb029300_T002) - p.Glu105Asp (EnsemblPlants:Zm00001eb029300_T001) - c.315G>C (EnsemblPlants:Zm00001eb029300_T001) Source type: large scale study Cross-references: | |||||||
PZE01154996192 | 112 | R>T | EnsemblPlants | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.03) Somatic: No Accession: 1:g.158673470C>G Codon: AGG/ACG Consequence type: missense Cytogenetic band: Genomic location: 1:g.158673470C>G Locations: - p.Arg112Thr (EnsemblPlants:Zm00001eb029300_T002) - c.335G>C (EnsemblPlants:Zm00001eb029300_T002) - p.Arg112Thr (EnsemblPlants:Zm00001eb029300_T001) - c.335G>C (EnsemblPlants:Zm00001eb029300_T001) Source type: large scale study Cross-references: | |||||||
PZE01154996049 | 160 | P>A | EnsemblPlants | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.25) Somatic: No Accession: 1:g.158673327G>C Codon: CCC/GCC Consequence type: missense Cytogenetic band: Genomic location: 1:g.158673327G>C Locations: - p.Pro160Ala (EnsemblPlants:Zm00001eb029300_T001) - c.478C>G (EnsemblPlants:Zm00001eb029300_T001) - p.Pro160Ala (EnsemblPlants:Zm00001eb029300_T002) - c.478C>G (EnsemblPlants:Zm00001eb029300_T002) Source type: large scale study Cross-references: | |||||||
PZE01154995902 | 209 | A>S | EnsemblPlants | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.63) Somatic: No Accession: 1:g.158673180C>A Codon: GCG/TCG Consequence type: missense Cytogenetic band: Genomic location: 1:g.158673180C>A Locations: - p.Ala209Ser (EnsemblPlants:Zm00001eb029300_T002) - c.625G>T (EnsemblPlants:Zm00001eb029300_T002) - p.Ala209Ser (EnsemblPlants:Zm00001eb029300_T001) - c.625G>T (EnsemblPlants:Zm00001eb029300_T001) Source type: large scale study Cross-references: | |||||||
PZE01154995868 | 220 | A>E | EnsemblPlants | ||||
Consequence: missense Predictions: - SIFT: tolerated (1) Somatic: No Accession: 1:g.158673146G>T Codon: GCG/GAG Consequence type: missense Cytogenetic band: Genomic location: 1:g.158673146G>T Locations: - p.Ala220Glu (EnsemblPlants:Zm00001eb029300_T002) - c.659C>A (EnsemblPlants:Zm00001eb029300_T002) - p.Ala220Glu (EnsemblPlants:Zm00001eb029300_T001) - c.659C>A (EnsemblPlants:Zm00001eb029300_T001) Source type: large scale study Cross-references: | |||||||
PZE01154995869 | 220 | A>P | EnsemblPlants | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.3) Somatic: No Accession: 1:g.158673147C>G Codon: GCG/CCG Consequence type: missense Cytogenetic band: Genomic location: 1:g.158673147C>G Locations: - p.Ala220Pro (EnsemblPlants:Zm00001eb029300_T002) - c.658G>C (EnsemblPlants:Zm00001eb029300_T002) - p.Ala220Pro (EnsemblPlants:Zm00001eb029300_T001) - c.658G>C (EnsemblPlants:Zm00001eb029300_T001) Source type: large scale study Cross-references: | |||||||
PZE01154995842 | 229 | S>P | EnsemblPlants | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.47) Somatic: No Accession: 1:g.158673120A>G Codon: TCG/CCG Consequence type: missense Cytogenetic band: Genomic location: 1:g.158673120A>G Locations: - p.Ser229Pro (EnsemblPlants:Zm00001eb029300_T001) - c.685T>C (EnsemblPlants:Zm00001eb029300_T001) - p.Ser229Pro (EnsemblPlants:Zm00001eb029300_T002) - c.685T>C (EnsemblPlants:Zm00001eb029300_T002) Source type: large scale study Cross-references: | |||||||
S1_154953416 | 266 | A>T | EnsemblPlants | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.24) Somatic: No Accession: 1:g.158673009C>T Codon: GCG/ACG Consequence type: missense Cytogenetic band: Genomic location: 1:g.158673009C>T Locations: - p.Ala266Thr (EnsemblPlants:Zm00001eb029300_T001) - c.796G>A (EnsemblPlants:Zm00001eb029300_T001) - p.Ala266Thr (EnsemblPlants:Zm00001eb029300_T002) - c.796G>A (EnsemblPlants:Zm00001eb029300_T002) Source type: large scale study Cross-references: | |||||||
S1_154953397 | 272 | A>V | EnsemblPlants | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.02) Somatic: No Accession: 1:g.158672990G>A Codon: GCG/GTG Consequence type: missense Cytogenetic band: Genomic location: 1:g.158672990G>A Locations: - p.Ala272Val (EnsemblPlants:Zm00001eb029300_T002) - c.815C>T (EnsemblPlants:Zm00001eb029300_T002) - p.Ala272Val (EnsemblPlants:Zm00001eb029300_T001) - c.815C>T (EnsemblPlants:Zm00001eb029300_T001) Source type: large scale study Cross-references: | |||||||
PZE01154995457 | 357 | G>A | EnsemblPlants | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.43) Somatic: No Accession: 1:g.158672735C>G Codon: GGG/GCG Consequence type: missense Cytogenetic band: Genomic location: 1:g.158672735C>G Locations: - p.Gly357Ala (EnsemblPlants:Zm00001eb029300_T002) - c.1070G>C (EnsemblPlants:Zm00001eb029300_T002) - p.Gly357Ala (EnsemblPlants:Zm00001eb029300_T001) - c.1070G>C (EnsemblPlants:Zm00001eb029300_T001) Source type: large scale study Cross-references: |