P31582 · RAF2A_ARATH
- ProteinRas-related protein RABF2a
- GeneRABF2A
- StatusUniProtKB reviewed (Swiss-Prot)
- Amino acids200 (go to sequence)
- Protein existenceEvidence at protein level
- Annotation score5/5
Variants
Variant ID(s) | Position(s) | Change | Description | Clinical significance | Provenance | ||
---|---|---|---|---|---|---|---|
tmp_5_18245079_C_T | 58 | T>I | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.07) Somatic: No Accession: 5:g.18245079C>T Codon: ACT/ATT Consequence type: missense Cytogenetic band: Genomic location: 5:g.18245079C>T Locations: - p.Thr58Ile (EnsemblPlants:AT5G45130.1) - c.173C>T (EnsemblPlants:AT5G45130.1) Source type: large scale study Cross-references: | |||||||
tmp_5_18245346_A_T | 103 | K>N | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.68) Somatic: No Accession: 5:g.18245346A>T Codon: AAA/AAT Consequence type: missense Cytogenetic band: Genomic location: 5:g.18245346A>T Locations: - p.Lys103Asn (EnsemblPlants:AT5G45130.1) - c.309A>T (EnsemblPlants:AT5G45130.1) Source type: large scale study Cross-references: | |||||||
ENSVATH07339874 | 105 | V>A | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 5:g.18245351T>C Codon: GTT/GCT Consequence type: missense Cytogenetic band: Genomic location: 5:g.18245351T>C Locations: - p.Val105Ala (EnsemblPlants:AT5G45130.1) - c.314T>C (EnsemblPlants:AT5G45130.1) Source type: large scale study Cross-references: | |||||||
ENSVATH00709257 | 139 | E>G | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.01) Somatic: No Accession: 5:g.18245775A>G Codon: GAG/GGG Consequence type: missense Cytogenetic band: Genomic location: 5:g.18245775A>G Locations: - p.Glu139Gly (EnsemblPlants:AT5G45130.1) - c.416A>G (EnsemblPlants:AT5G45130.1) Source type: large scale study Cross-references: | |||||||
ENSVATH12538201 | 173 | R>L | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.2) Somatic: No Accession: 5:g.18245975G>T Codon: CGT/CTT Consequence type: missense Cytogenetic band: Genomic location: 5:g.18245975G>T Locations: - p.Arg173Leu (EnsemblPlants:AT5G45130.1) - c.518G>T (EnsemblPlants:AT5G45130.1) Source type: large scale study Cross-references: | |||||||
ENSVATH12538202 | 197 | S>P | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.29) Somatic: No Accession: 5:g.18246046T>C Codon: TCG/CCG Consequence type: missense Cytogenetic band: Genomic location: 5:g.18246046T>C Locations: - p.Ser197Pro (EnsemblPlants:AT5G45130.1) - c.589T>C (EnsemblPlants:AT5G45130.1) Source type: large scale study Cross-references: |