Q9SKN7 · SMR11_ARATH
- ProteinCyclin-dependent protein kinase inhibitor SMR11
- GeneSMR11
- StatusUniProtKB reviewed (Swiss-Prot)
- Amino acids154 (go to sequence)
- Protein existenceEvidence at protein level
- Annotation score2/5
Variants
Variant ID(s) | Position(s) | Change | Description | Clinical significance | Provenance | ||
---|---|---|---|---|---|---|---|
tmp_2_12100536_T_A | 30 | I>F | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated - low confidence (0.22) Somatic: No Accession: 2:g.12100536T>A Codon: ATT/TTT Consequence type: missense Cytogenetic band: Genomic location: 2:g.12100536T>A Locations: - p.Ile30Phe (EnsemblPlants:AT2G28330.1) - c.88A>T (EnsemblPlants:AT2G28330.1) Source type: large scale study Cross-references: | |||||||
tmp_2_12100493_A_T | 44 | I>K | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.94) Somatic: No Accession: 2:g.12100493A>T Codon: ATA/AAA Consequence type: missense Cytogenetic band: Genomic location: 2:g.12100493A>T Locations: - p.Ile44Lys (EnsemblPlants:AT2G28330.1) - c.131T>A (EnsemblPlants:AT2G28330.1) Source type: large scale study Cross-references: | |||||||
ENSVATH05612258 | 45 | V>A | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.61) Somatic: No Accession: 2:g.12100490A>G Codon: GTT/GCT Consequence type: missense Cytogenetic band: Genomic location: 2:g.12100490A>G Locations: - p.Val45Ala (EnsemblPlants:AT2G28330.1) - c.134T>C (EnsemblPlants:AT2G28330.1) Source type: large scale study Cross-references: | |||||||
ENSVATH05612259 | 45 | V>I | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.83) Somatic: No Accession: 2:g.12100491C>T Codon: GTT/ATT Consequence type: missense Cytogenetic band: Genomic location: 2:g.12100491C>T Locations: - p.Val45Ile (EnsemblPlants:AT2G28330.1) - c.133G>A (EnsemblPlants:AT2G28330.1) Source type: large scale study Cross-references: | |||||||
ENSVATH01913687 | 47 | E>D | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.63) Somatic: No Accession: 2:g.12100483C>A Codon: GAG/GAT Consequence type: missense Cytogenetic band: Genomic location: 2:g.12100483C>A Locations: - p.Glu47Asp (EnsemblPlants:AT2G28330.1) - c.141G>T (EnsemblPlants:AT2G28330.1) Source type: large scale study Cross-references: | |||||||
tmp_2_12100448_C_T | 59 | C>Y | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.05) Somatic: No Accession: 2:g.12100448C>T Codon: TGT/TAT Consequence type: missense Cytogenetic band: Genomic location: 2:g.12100448C>T Locations: - p.Cys59Tyr (EnsemblPlants:AT2G28330.1) - c.176G>A (EnsemblPlants:AT2G28330.1) Source type: large scale study Cross-references: | |||||||
ENSVATH05612255 | 64 | D>Y | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 2:g.12100434C>A Codon: GAT/TAT Consequence type: missense Cytogenetic band: Genomic location: 2:g.12100434C>A Locations: - p.Asp64Tyr (EnsemblPlants:AT2G28330.1) - c.190G>T (EnsemblPlants:AT2G28330.1) Source type: large scale study Cross-references: | |||||||
ENSVATH13446367 | 76 | D>N | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 2:g.12100398C>T Codon: GAT/AAT Consequence type: missense Cytogenetic band: Genomic location: 2:g.12100398C>T Locations: - p.Asp76Asn (EnsemblPlants:AT2G28330.1) - c.226G>A (EnsemblPlants:AT2G28330.1) Source type: large scale study Cross-references: | |||||||
tmp_2_12100310_T_C | 105 | E>G | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.08) Somatic: No Accession: 2:g.12100310T>C Codon: GAG/GGG Consequence type: missense Cytogenetic band: Genomic location: 2:g.12100310T>C Locations: - p.Glu105Gly (EnsemblPlants:AT2G28330.1) - c.314A>G (EnsemblPlants:AT2G28330.1) Source type: large scale study Cross-references: | |||||||
ENSVATH05612254 | 119 | S>F | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.42) Somatic: No Accession: 2:g.12100268G>A Codon: TCT/TTT Consequence type: missense Cytogenetic band: Genomic location: 2:g.12100268G>A Locations: - p.Ser119Phe (EnsemblPlants:AT2G28330.1) - c.356C>T (EnsemblPlants:AT2G28330.1) Source type: large scale study Cross-references: | |||||||
tmp_2_12100265_C_T | 120 | R>Q | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.26) Somatic: No Accession: 2:g.12100265C>T Codon: CGG/CAG Consequence type: missense Cytogenetic band: Genomic location: 2:g.12100265C>T Locations: - p.Arg120Gln (EnsemblPlants:AT2G28330.1) - c.359G>A (EnsemblPlants:AT2G28330.1) Source type: large scale study Cross-references: | |||||||
ENSVATH05612253 | 136 | M>L | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.45) Somatic: No Accession: 2:g.12100218T>A Codon: ATG/TTG Consequence type: missense Cytogenetic band: Genomic location: 2:g.12100218T>A Locations: - p.Met136Leu (EnsemblPlants:AT2G28330.1) - c.406A>T (EnsemblPlants:AT2G28330.1) Source type: large scale study Cross-references: |