Q43735 · PER27_ARATH
- ProteinPeroxidase 27
- GenePER27
- StatusUniProtKB reviewed (Swiss-Prot)
- Amino acids321 (go to sequence)
- Protein existenceEvidence at protein level
- Annotation score5/5
Variants
Variant ID(s) | Position(s) | Change | Description | Clinical significance | Provenance | ||
---|---|---|---|---|---|---|---|
tmp_3_68467_G_GCTT | 4 | S>* | 1000Genomes | ||||
Consequence: stop gained Somatic: No Accession: 3:g.68467_68468insCTT Codon: TCT/TAAGCT Consequence type: stop gained Cytogenetic band: Genomic location: 3:g.68467_68468insCTT Locations: - p.Ser4delinsTer (EnsemblPlants:AT3G01190.1) - c.10_11insAAG (EnsemblPlants:AT3G01190.1) Source type: large scale study Cross-references: | |||||||
ENSVATH10447053 | 4 | S>P | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.15) Somatic: No Accession: 3:g.68468A>G Codon: TCT/CCT Consequence type: missense Cytogenetic band: Genomic location: 3:g.68468A>G Locations: - p.Ser4Pro (EnsemblPlants:AT3G01190.1) - c.10T>C (EnsemblPlants:AT3G01190.1) Source type: large scale study Cross-references: | |||||||
ENSVATH10447051 | 6 | R>Q | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.31) Somatic: No Accession: 3:g.68461C>T Codon: CGA/CAA Consequence type: missense Cytogenetic band: Genomic location: 3:g.68461C>T Locations: - p.Arg6Gln (EnsemblPlants:AT3G01190.1) - c.17G>A (EnsemblPlants:AT3G01190.1) Source type: large scale study Cross-references: | |||||||
tmp_3_68446_C_T | 11 | C>Y | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.17) Somatic: No Accession: 3:g.68446C>T Codon: TGC/TAC Consequence type: missense Cytogenetic band: Genomic location: 3:g.68446C>T Locations: - p.Cys11Tyr (EnsemblPlants:AT3G01190.1) - c.32G>A (EnsemblPlants:AT3G01190.1) Source type: large scale study Cross-references: | |||||||
tmp_3_68367_T_A | 37 | Q>H | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.21) Somatic: No Accession: 3:g.68367T>A Codon: CAA/CAT Consequence type: missense Cytogenetic band: Genomic location: 3:g.68367T>A Locations: - p.Gln37His (EnsemblPlants:AT3G01190.1) - c.111A>T (EnsemblPlants:AT3G01190.1) Source type: large scale study Cross-references: | |||||||
ENSVATH10447049 | 84 | N>S | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.12) Somatic: No Accession: 3:g.68132T>C Codon: AAT/AGT Consequence type: missense Cytogenetic band: Genomic location: 3:g.68132T>C Locations: - p.Asn84Ser (EnsemblPlants:AT3G01190.1) - c.251A>G (EnsemblPlants:AT3G01190.1) Source type: large scale study Cross-references: | |||||||
tmp_3_67848_C_T | 146 | R>K | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.06) Somatic: No Accession: 3:g.67848C>T Codon: AGA/AAA Consequence type: missense Cytogenetic band: Genomic location: 3:g.67848C>T Locations: - p.Arg146Lys (EnsemblPlants:AT3G01190.1) - c.437G>A (EnsemblPlants:AT3G01190.1) Source type: large scale study Cross-references: | |||||||
ENSVATH13855090 | 150 | V>G | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.01) Somatic: No Accession: 3:g.67836A>C Codon: GTT/GGT Consequence type: missense Cytogenetic band: Genomic location: 3:g.67836A>C Locations: - p.Val150Gly (EnsemblPlants:AT3G01190.1) - c.449T>G (EnsemblPlants:AT3G01190.1) Source type: large scale study Cross-references: | |||||||
tmp_3_67396_A_C | 269 | L>R | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 3:g.67396A>C Codon: CTC/CGC Consequence type: missense Cytogenetic band: Genomic location: 3:g.67396A>C Locations: - p.Leu269Arg (EnsemblPlants:AT3G01190.1) - c.806T>G (EnsemblPlants:AT3G01190.1) Source type: large scale study Cross-references: | |||||||
tmp_3_67326_G_C | 292 | D>E | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.66) Somatic: No Accession: 3:g.67326G>C Codon: GAC/GAG Consequence type: missense Cytogenetic band: Genomic location: 3:g.67326G>C Locations: - p.Asp292Glu (EnsemblPlants:AT3G01190.1) - c.876C>G (EnsemblPlants:AT3G01190.1) Source type: large scale study Cross-references: | |||||||
ENSVATH13855087 | 311 | G>W | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 3:g.67271C>A Codon: GGG/TGG Consequence type: missense Cytogenetic band: Genomic location: 3:g.67271C>A Locations: - p.Gly311Trp (EnsemblPlants:AT3G01190.1) - c.931G>T (EnsemblPlants:AT3G01190.1) Source type: large scale study Cross-references: |