O82204 · RL281_ARATH
- ProteinLarge ribosomal subunit protein eL28z
- GeneRPL28A
- StatusUniProtKB reviewed (Swiss-Prot)
- Amino acids143 (go to sequence)
- Protein existenceEvidence at protein level
- Annotation score5/5
Variants
Variant ID(s) | Position(s) | Change | Description | Clinical significance | Provenance | ||
---|---|---|---|---|---|---|---|
ENSVATH05535764 | 2 | A>V | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.15) Somatic: No Accession: 2:g.8511756C>T Codon: GCG/GTG Consequence type: missense Cytogenetic band: Genomic location: 2:g.8511756C>T Locations: - p.Ala2Val (EnsemblPlants:AT2G19730.3) - c.5C>T (EnsemblPlants:AT2G19730.3) - p.Ala2Val (EnsemblPlants:AT2G19730.1) - c.5C>T (EnsemblPlants:AT2G19730.1) - p.Ala2Val (EnsemblPlants:AT2G19730.2) - c.5C>T (EnsemblPlants:AT2G19730.2) Source type: large scale study Cross-references: | |||||||
ENSVATH05535765 | 14 | K>N | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 2:g.8511793G>T Codon: AAG/AAT Consequence type: missense Cytogenetic band: Genomic location: 2:g.8511793G>T Locations: - p.Lys14Asn (EnsemblPlants:AT2G19730.3) - c.42G>T (EnsemblPlants:AT2G19730.3) - p.Lys14Asn (EnsemblPlants:AT2G19730.1) - c.42G>T (EnsemblPlants:AT2G19730.1) - p.Lys14Asn (EnsemblPlants:AT2G19730.2) - c.42G>T (EnsemblPlants:AT2G19730.2) Source type: large scale study Cross-references: | |||||||
ENSVATH05535791 | 65 | D>E | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.18) Somatic: No Accession: 2:g.8512416C>A Codon: GAC/GAA Consequence type: missense Cytogenetic band: Genomic location: 2:g.8512416C>A Locations: - p.Asp65Glu (EnsemblPlants:AT2G19730.3) - c.195C>A (EnsemblPlants:AT2G19730.3) - p.Asp65Glu (EnsemblPlants:AT2G19730.1) - c.195C>A (EnsemblPlants:AT2G19730.1) - p.Asp65Glu (EnsemblPlants:AT2G19730.2) - c.195C>A (EnsemblPlants:AT2G19730.2) Source type: large scale study Cross-references: | |||||||
ENSVATH05535792 | 83 | L>H | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.05) Somatic: No Accession: 2:g.8512469T>A Codon: CTC/CAC Consequence type: missense Cytogenetic band: Genomic location: 2:g.8512469T>A Locations: - p.Leu83His (EnsemblPlants:AT2G19730.3) - c.248T>A (EnsemblPlants:AT2G19730.3) - p.Leu83His (EnsemblPlants:AT2G19730.1) - c.248T>A (EnsemblPlants:AT2G19730.1) - p.Leu83His (EnsemblPlants:AT2G19730.2) - c.248T>A (EnsemblPlants:AT2G19730.2) Source type: large scale study Cross-references: | |||||||
tmp_2_8512483_T_A | 88 | S>T | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.37) Somatic: No Accession: 2:g.8512483T>A Codon: TCT/ACT Consequence type: missense Cytogenetic band: Genomic location: 2:g.8512483T>A Locations: - p.Ser88Thr (EnsemblPlants:AT2G19730.3) - c.262T>A (EnsemblPlants:AT2G19730.3) - p.Ser88Thr (EnsemblPlants:AT2G19730.1) - c.262T>A (EnsemblPlants:AT2G19730.1) - p.Ser88Thr (EnsemblPlants:AT2G19730.2) - c.262T>A (EnsemblPlants:AT2G19730.2) Source type: large scale study Cross-references: | |||||||
ENSVATH01846343 | 89 | I>T | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.38) Somatic: No Accession: 2:g.8512487T>C Codon: ATC/ACC Consequence type: missense Cytogenetic band: Genomic location: 2:g.8512487T>C Locations: - p.Ile89Thr (EnsemblPlants:AT2G19730.3) - c.266T>C (EnsemblPlants:AT2G19730.3) - p.Ile89Thr (EnsemblPlants:AT2G19730.1) - c.266T>C (EnsemblPlants:AT2G19730.1) - p.Ile89Thr (EnsemblPlants:AT2G19730.2) - c.266T>C (EnsemblPlants:AT2G19730.2) Source type: large scale study Cross-references: | |||||||
ENSVATH13285795 | 96 | R>G | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 2:g.8512507A>G Codon: AGG/GGG Consequence type: missense Cytogenetic band: Genomic location: 2:g.8512507A>G Locations: - p.Arg96Gly (EnsemblPlants:AT2G19730.3) - c.286A>G (EnsemblPlants:AT2G19730.3) - p.Arg96Gly (EnsemblPlants:AT2G19730.1) - c.286A>G (EnsemblPlants:AT2G19730.1) - p.Arg96Gly (EnsemblPlants:AT2G19730.2) - c.286A>G (EnsemblPlants:AT2G19730.2) Source type: large scale study Cross-references: | |||||||
tmp_2_8512940_G_C | 126 | S>T | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.01) Somatic: No Accession: 2:g.8512940G>C Codon: AGC/ACC Consequence type: missense Cytogenetic band: Genomic location: 2:g.8512940G>C Locations: - p.Ser126Thr (EnsemblPlants:AT2G19730.3) - c.377G>C (EnsemblPlants:AT2G19730.3) - p.Ser126Thr (EnsemblPlants:AT2G19730.1) - c.377G>C (EnsemblPlants:AT2G19730.1) - p.Ser126Thr (EnsemblPlants:AT2G19730.2) - c.377G>C (EnsemblPlants:AT2G19730.2) Source type: large scale study Cross-references: |