Q9SCS2 · CAMK5_ARATH
- ProteinCDPK-related kinase 5
- GeneCRK5
- StatusUniProtKB reviewed (Swiss-Prot)
- Amino acids601 (go to sequence)
- Protein existenceEvidence at transcript level
- Annotation score5/5
Variants
Variant ID(s) | Position(s) | Change | Description | Clinical significance | Provenance | ||
---|---|---|---|---|---|---|---|
tmp_3_18753974_A_T | 48 | N>Y | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.03) Somatic: No Accession: 3:g.18753974A>T Codon: AAT/TAT Consequence type: missense Cytogenetic band: Genomic location: 3:g.18753974A>T Locations: - p.Asn48Tyr (EnsemblPlants:AT3G50530.1) - c.142A>T (EnsemblPlants:AT3G50530.1) Source type: large scale study Cross-references: | |||||||
tmp_3_18754103_A_C | 91 | K>Q | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.03) Somatic: No Accession: 3:g.18754103A>C Codon: AAA/CAA Consequence type: missense Cytogenetic band: Genomic location: 3:g.18754103A>C Locations: - p.Lys91Gln (EnsemblPlants:AT3G50530.1) - c.271A>C (EnsemblPlants:AT3G50530.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06287552 | 129 | G>R | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.4) Somatic: No Accession: 3:g.18754217G>A Codon: GGA/AGA Consequence type: missense Cytogenetic band: Genomic location: 3:g.18754217G>A Locations: - p.Gly129Arg (EnsemblPlants:AT3G50530.1) - c.385G>A (EnsemblPlants:AT3G50530.1) Source type: large scale study Cross-references: | |||||||
tmp_3_18754218_G_T | 129 | G>V | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.19) Somatic: No Accession: 3:g.18754218G>T Codon: GGA/GTA Consequence type: missense Cytogenetic band: Genomic location: 3:g.18754218G>T Locations: - p.Gly129Val (EnsemblPlants:AT3G50530.1) - c.386G>T (EnsemblPlants:AT3G50530.1) Source type: large scale study Cross-references: | |||||||
tmp_3_18754258_G_T | 142 | K>N | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.04) Somatic: No Accession: 3:g.18754258G>T Codon: AAG/AAT Consequence type: missense Cytogenetic band: Genomic location: 3:g.18754258G>T Locations: - p.Lys142Asn (EnsemblPlants:AT3G50530.1) - c.426G>T (EnsemblPlants:AT3G50530.1) Source type: large scale study Cross-references: | |||||||
ENSVATH00413081 | 303 | Y>F | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (1) Somatic: No Accession: 3:g.18755094A>T Codon: TAC/TTC Consequence type: missense Cytogenetic band: Genomic location: 3:g.18755094A>T Locations: - p.Tyr303Phe (EnsemblPlants:AT3G50530.1) - c.908A>T (EnsemblPlants:AT3G50530.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06287567 | 351 | P>L | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 3:g.18755331C>T Codon: CCG/CTG Consequence type: missense Cytogenetic band: Genomic location: 3:g.18755331C>T Locations: - p.Pro351Leu (EnsemblPlants:AT3G50530.1) - c.1052C>T (EnsemblPlants:AT3G50530.1) Source type: large scale study Cross-references: | |||||||
tmp_3_18755445_G_A | 389 | R>Q | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.01) Somatic: No Accession: 3:g.18755445G>A Codon: CGG/CAG Consequence type: missense Cytogenetic band: Genomic location: 3:g.18755445G>A Locations: - p.Arg389Gln (EnsemblPlants:AT3G50530.1) - c.1166G>A (EnsemblPlants:AT3G50530.1) Source type: large scale study Cross-references: | |||||||
ENSVATH12690255 | 411 | K>R | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (1) Somatic: No Accession: 3:g.18755578A>G Codon: AAG/AGG Consequence type: missense Cytogenetic band: Genomic location: 3:g.18755578A>G Locations: - p.Lys411Arg (EnsemblPlants:AT3G50530.1) - c.1232A>G (EnsemblPlants:AT3G50530.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06287570 | 427 | L>I | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.17) Somatic: No Accession: 3:g.18755625C>A Codon: CTT/ATT Consequence type: missense Cytogenetic band: Genomic location: 3:g.18755625C>A Locations: - p.Leu427Ile (EnsemblPlants:AT3G50530.1) - c.1279C>A (EnsemblPlants:AT3G50530.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06287574 | 451 | V>A | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.25) Somatic: No Accession: 3:g.18755775T>C Codon: GTT/GCT Consequence type: missense Cytogenetic band: Genomic location: 3:g.18755775T>C Locations: - p.Val451Ala (EnsemblPlants:AT3G50530.1) - c.1352T>C (EnsemblPlants:AT3G50530.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06287573 | 451 | V>F | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.02) Somatic: No Accession: 3:g.18755774G>T Codon: GTT/TTT Consequence type: missense Cytogenetic band: Genomic location: 3:g.18755774G>T Locations: - p.Val451Phe (EnsemblPlants:AT3G50530.1) - c.1351G>T (EnsemblPlants:AT3G50530.1) Source type: large scale study Cross-references: | |||||||
ENSVATH12690257 | 455 | F>C | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.18) Somatic: No Accession: 3:g.18755787T>G Codon: TTT/TGT Consequence type: missense Cytogenetic band: Genomic location: 3:g.18755787T>G Locations: - p.Phe455Cys (EnsemblPlants:AT3G50530.1) - c.1364T>G (EnsemblPlants:AT3G50530.1) Source type: large scale study Cross-references: | |||||||
tmp_3_18756125_G_A | 510 | D>N | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.01) Somatic: No Accession: 3:g.18756125G>A Codon: GAC/AAC Consequence type: missense Cytogenetic band: Genomic location: 3:g.18756125G>A Locations: - p.Asp510Asn (EnsemblPlants:AT3G50530.1) - c.1528G>A (EnsemblPlants:AT3G50530.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06287577 | 523 | Q>K | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.06) Somatic: No Accession: 3:g.18756164C>A Codon: CAG/AAG Consequence type: missense Cytogenetic band: Genomic location: 3:g.18756164C>A Locations: - p.Gln523Lys (EnsemblPlants:AT3G50530.1) - c.1567C>A (EnsemblPlants:AT3G50530.1) Source type: large scale study Cross-references: | |||||||
tmp_3_18756251_G_A | 552 | D>N | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 3:g.18756251G>A Codon: GAT/AAT Consequence type: missense Cytogenetic band: Genomic location: 3:g.18756251G>A Locations: - p.Asp552Asn (EnsemblPlants:AT3G50530.1) - c.1654G>A (EnsemblPlants:AT3G50530.1) Source type: large scale study Cross-references: | |||||||
tmp_3_18756369_C_T | 563 | S>F | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.01) Somatic: No Accession: 3:g.18756369C>T Codon: TCT/TTT Consequence type: missense Cytogenetic band: Genomic location: 3:g.18756369C>T Locations: - p.Ser563Phe (EnsemblPlants:AT3G50530.1) - c.1688C>T (EnsemblPlants:AT3G50530.1) Source type: large scale study Cross-references: | |||||||
tmp_3_18756368_T_A | 563 | S>T | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.16) Somatic: No Accession: 3:g.18756368T>A Codon: TCT/ACT Consequence type: missense Cytogenetic band: Genomic location: 3:g.18756368T>A Locations: - p.Ser563Thr (EnsemblPlants:AT3G50530.1) - c.1687T>A (EnsemblPlants:AT3G50530.1) Source type: large scale study Cross-references: |