Q93WK5 · APRR7_ARATH
- ProteinTwo-component response regulator-like APRR7
- GeneAPRR7
- StatusUniProtKB reviewed (Swiss-Prot)
- Amino acids727 (go to sequence)
- Protein existenceEvidence at protein level
- Annotation score5/5
Variants
Variant ID(s) | Position(s) | Change | Description | Clinical significance | Provenance | ||
---|---|---|---|---|---|---|---|
tmp_5_641442_C_T | 7 | G>E | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious - low confidence (0.03) Somatic: No Accession: 5:g.641442C>T Codon: GGG/GAG Consequence type: missense Cytogenetic band: Genomic location: 5:g.641442C>T Locations: - p.Gly7Glu (EnsemblPlants:AT5G02810.1) - c.20G>A (EnsemblPlants:AT5G02810.1) Source type: large scale study Cross-references: | |||||||
tmp_5_641409_T_A | 18 | K>M | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious - low confidence (0.02) Somatic: No Accession: 5:g.641409T>A Codon: AAG/ATG Consequence type: missense Cytogenetic band: Genomic location: 5:g.641409T>A Locations: - p.Lys18Met (EnsemblPlants:AT5G02810.1) - c.53A>T (EnsemblPlants:AT5G02810.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06911236 | 40 | T>I | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.43) Somatic: No Accession: 5:g.641343G>A Codon: ACT/ATT Consequence type: missense Cytogenetic band: Genomic location: 5:g.641343G>A Locations: - p.Thr40Ile (EnsemblPlants:AT5G02810.1) - c.119C>T (EnsemblPlants:AT5G02810.1) Source type: large scale study Cross-references: | |||||||
ENSVATH03011230 | 47 | V>G | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 5:g.641322A>C Codon: GTG/GGG Consequence type: missense Cytogenetic band: Genomic location: 5:g.641322A>C Locations: - p.Val47Gly (EnsemblPlants:AT5G02810.1) - c.140T>G (EnsemblPlants:AT5G02810.1) Source type: large scale study Cross-references: | |||||||
ENSVATH00602672 | 63 | T>S | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.75) Somatic: No Accession: 5:g.641275T>A Codon: ACA/TCA Consequence type: missense Cytogenetic band: Genomic location: 5:g.641275T>A Locations: - p.Thr63Ser (EnsemblPlants:AT5G02810.1) - c.187A>T (EnsemblPlants:AT5G02810.1) Source type: large scale study Cross-references: | |||||||
ENSVATH10512730 | 65 | A>T | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.06) Somatic: No Accession: 5:g.641269C>T Codon: GCA/ACA Consequence type: missense Cytogenetic band: Genomic location: 5:g.641269C>T Locations: - p.Ala65Thr (EnsemblPlants:AT5G02810.1) - c.193G>A (EnsemblPlants:AT5G02810.1) Source type: large scale study Cross-references: | |||||||
tmp_5_640413_G_A | 215 | T>I | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.04) Somatic: No Accession: 5:g.640413G>A Codon: ACT/ATT Consequence type: missense Cytogenetic band: Genomic location: 5:g.640413G>A Locations: - p.Thr215Ile (EnsemblPlants:AT5G02810.1) - c.644C>T (EnsemblPlants:AT5G02810.1) Source type: large scale study Cross-references: | |||||||
ENSVATH13888847 | 216 | Q>E | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.01) Somatic: No Accession: 5:g.640411G>C Codon: CAA/GAA Consequence type: missense Cytogenetic band: Genomic location: 5:g.640411G>C Locations: - p.Gln216Glu (EnsemblPlants:AT5G02810.1) - c.646C>G (EnsemblPlants:AT5G02810.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06911224 | 245 | N>T | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.01) Somatic: No Accession: 5:g.640323T>G Codon: AAT/ACT Consequence type: missense Cytogenetic band: Genomic location: 5:g.640323T>G Locations: - p.Asn245Thr (EnsemblPlants:AT5G02810.1) - c.734A>C (EnsemblPlants:AT5G02810.1) Source type: large scale study Cross-references: | |||||||
tmp_5_639881_G_A | 295 | P>L | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.68) Somatic: No Accession: 5:g.639881G>A Codon: CCA/CTA Consequence type: missense Cytogenetic band: Genomic location: 5:g.639881G>A Locations: - p.Pro295Leu (EnsemblPlants:AT5G02810.1) - c.884C>T (EnsemblPlants:AT5G02810.1) Source type: large scale study Cross-references: | |||||||
ENSVATH00602665 | 301 | A>V | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.12) Somatic: No Accession: 5:g.639863G>A Codon: GCA/GTA Consequence type: missense Cytogenetic band: Genomic location: 5:g.639863G>A Locations: - p.Ala301Val (EnsemblPlants:AT5G02810.1) - c.902C>T (EnsemblPlants:AT5G02810.1) Source type: large scale study Cross-references: | |||||||
ENSVATH13888845 | 313 | D>N | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.09) Somatic: No Accession: 5:g.639828C>T Codon: GAT/AAT Consequence type: missense Cytogenetic band: Genomic location: 5:g.639828C>T Locations: - p.Asp313Asn (EnsemblPlants:AT5G02810.1) - c.937G>A (EnsemblPlants:AT5G02810.1) Source type: large scale study Cross-references: | |||||||
ENSVATH00602664 | 333 | D>N | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.32) Somatic: No Accession: 5:g.639670C>T Codon: GAT/AAT Consequence type: missense Cytogenetic band: Genomic location: 5:g.639670C>T Locations: - p.Asp333Asn (EnsemblPlants:AT5G02810.1) - c.997G>A (EnsemblPlants:AT5G02810.1) Source type: large scale study Cross-references: | |||||||
tmp_5_639664_C_T | 335 | A>T | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.05) Somatic: No Accession: 5:g.639664C>T Codon: GCC/ACC Consequence type: missense Cytogenetic band: Genomic location: 5:g.639664C>T Locations: - p.Ala335Thr (EnsemblPlants:AT5G02810.1) - c.1003G>A (EnsemblPlants:AT5G02810.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06911214 | 339 | K>R | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.49) Somatic: No Accession: 5:g.639651T>C Codon: AAA/AGA Consequence type: missense Cytogenetic band: Genomic location: 5:g.639651T>C Locations: - p.Lys339Arg (EnsemblPlants:AT5G02810.1) - c.1016A>G (EnsemblPlants:AT5G02810.1) Source type: large scale study Cross-references: | |||||||
tmp_5_639644_T_A | 341 | E>D | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.27) Somatic: No Accession: 5:g.639644T>A Codon: GAA/GAT Consequence type: missense Cytogenetic band: Genomic location: 5:g.639644T>A Locations: - p.Glu341Asp (EnsemblPlants:AT5G02810.1) - c.1023A>T (EnsemblPlants:AT5G02810.1) Source type: large scale study Cross-references: | |||||||
ENSVATH03011223 | 342 | P>L | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.32) Somatic: No Accession: 5:g.639642G>A Codon: CCC/CTC Consequence type: missense Cytogenetic band: Genomic location: 5:g.639642G>A Locations: - p.Pro342Leu (EnsemblPlants:AT5G02810.1) - c.1025C>T (EnsemblPlants:AT5G02810.1) Source type: large scale study Cross-references: | |||||||
ENSVATH00602663 | 346 | T>I | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.41) Somatic: No Accession: 5:g.639630G>A Codon: ACT/ATT Consequence type: missense Cytogenetic band: Genomic location: 5:g.639630G>A Locations: - p.Thr346Ile (EnsemblPlants:AT5G02810.1) - c.1037C>T (EnsemblPlants:AT5G02810.1) Source type: large scale study Cross-references: | |||||||
tmp_5_639592_T_C | 359 | S>G | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.54) Somatic: No Accession: 5:g.639592T>C Codon: AGC/GGC Consequence type: missense Cytogenetic band: Genomic location: 5:g.639592T>C Locations: - p.Ser359Gly (EnsemblPlants:AT5G02810.1) - c.1075A>G (EnsemblPlants:AT5G02810.1) Source type: large scale study Cross-references: | |||||||
tmp_5_639555_G_A | 371 | P>L | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.18) Somatic: No Accession: 5:g.639555G>A Codon: CCA/CTA Consequence type: missense Cytogenetic band: Genomic location: 5:g.639555G>A Locations: - p.Pro371Leu (EnsemblPlants:AT5G02810.1) - c.1112C>T (EnsemblPlants:AT5G02810.1) Source type: large scale study Cross-references: | |||||||
tmp_5_639546_A_T | 374 | L>H | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.24) Somatic: No Accession: 5:g.639546A>T Codon: CTC/CAC Consequence type: missense Cytogenetic band: Genomic location: 5:g.639546A>T Locations: - p.Leu374His (EnsemblPlants:AT5G02810.1) - c.1121T>A (EnsemblPlants:AT5G02810.1) Source type: large scale study Cross-references: | |||||||
tmp_5_639499_A_G | 390 | S>P | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.16) Somatic: No Accession: 5:g.639499A>G Codon: TCG/CCG Consequence type: missense Cytogenetic band: Genomic location: 5:g.639499A>G Locations: - p.Ser390Pro (EnsemblPlants:AT5G02810.1) - c.1168T>C (EnsemblPlants:AT5G02810.1) Source type: large scale study Cross-references: | |||||||
ENSVATH00602662 | 408 | P>L | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.1) Somatic: No Accession: 5:g.639444G>A Codon: CCT/CTT Consequence type: missense Cytogenetic band: Genomic location: 5:g.639444G>A Locations: - p.Pro408Leu (EnsemblPlants:AT5G02810.1) - c.1223C>T (EnsemblPlants:AT5G02810.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06911212 | 413 | K>E | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.06) Somatic: No Accession: 5:g.639430T>C Codon: AAA/GAA Consequence type: missense Cytogenetic band: Genomic location: 5:g.639430T>C Locations: - p.Lys413Glu (EnsemblPlants:AT5G02810.1) - c.1237A>G (EnsemblPlants:AT5G02810.1) Source type: large scale study Cross-references: | |||||||
tmp_5_639427_T_G | 414 | T>P | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.08) Somatic: No Accession: 5:g.639427T>G Codon: ACT/CCT Consequence type: missense Cytogenetic band: Genomic location: 5:g.639427T>G Locations: - p.Thr414Pro (EnsemblPlants:AT5G02810.1) - c.1240A>C (EnsemblPlants:AT5G02810.1) Source type: large scale study Cross-references: | |||||||
tmp_5_639422_T_G | 415 | L>F | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.25) Somatic: No Accession: 5:g.639422T>G Codon: TTA/TTC Consequence type: missense Cytogenetic band: Genomic location: 5:g.639422T>G Locations: - p.Leu415Phe (EnsemblPlants:AT5G02810.1) - c.1245A>C (EnsemblPlants:AT5G02810.1) Source type: large scale study Cross-references: | |||||||
tmp_5_639379_G_T | 430 | H>N | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.08) Somatic: No Accession: 5:g.639379G>T Codon: CAC/AAC Consequence type: missense Cytogenetic band: Genomic location: 5:g.639379G>T Locations: - p.His430Asn (EnsemblPlants:AT5G02810.1) - c.1288C>A (EnsemblPlants:AT5G02810.1) Source type: large scale study Cross-references: | |||||||
tmp_5_639366_C_T | 434 | S>N | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.02) Somatic: No Accession: 5:g.639366C>T Codon: AGT/AAT Consequence type: missense Cytogenetic band: Genomic location: 5:g.639366C>T Locations: - p.Ser434Asn (EnsemblPlants:AT5G02810.1) - c.1301G>A (EnsemblPlants:AT5G02810.1) Source type: large scale study Cross-references: | |||||||
tmp_5_639158_T_C | 471 | N>S | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.44) Somatic: No Accession: 5:g.639158T>C Codon: AAT/AGT Consequence type: missense Cytogenetic band: Genomic location: 5:g.639158T>C Locations: - p.Asn471Ser (EnsemblPlants:AT5G02810.1) - c.1412A>G (EnsemblPlants:AT5G02810.1) Source type: large scale study Cross-references: | |||||||
ENSVATH00602660 | 478 | G>E | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.02) Somatic: No Accession: 5:g.639137C>T Codon: GGG/GAG Consequence type: missense Cytogenetic band: Genomic location: 5:g.639137C>T Locations: - p.Gly478Glu (EnsemblPlants:AT5G02810.1) - c.1433G>A (EnsemblPlants:AT5G02810.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06911204 | 497 | T>N | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.05) Somatic: No Accession: 5:g.639080G>T Codon: ACT/AAT Consequence type: missense Cytogenetic band: Genomic location: 5:g.639080G>T Locations: - p.Thr497Asn (EnsemblPlants:AT5G02810.1) - c.1490C>A (EnsemblPlants:AT5G02810.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06911203 | 498 | E>V | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.12) Somatic: No Accession: 5:g.639077T>A Codon: GAA/GTA Consequence type: missense Cytogenetic band: Genomic location: 5:g.639077T>A Locations: - p.Glu498Val (EnsemblPlants:AT5G02810.1) - c.1493A>T (EnsemblPlants:AT5G02810.1) Source type: large scale study Cross-references: | |||||||
tmp_5_639027_G_T | 515 | H>N | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.12) Somatic: No Accession: 5:g.639027G>T Codon: CAT/AAT Consequence type: missense Cytogenetic band: Genomic location: 5:g.639027G>T Locations: - p.His515Asn (EnsemblPlants:AT5G02810.1) - c.1543C>A (EnsemblPlants:AT5G02810.1) Source type: large scale study Cross-references: | |||||||
ENSVATH00602658 | 572 | L>H | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.56) Somatic: No Accession: 5:g.638855A>T Codon: CTT/CAT Consequence type: missense Cytogenetic band: Genomic location: 5:g.638855A>T Locations: - p.Leu572His (EnsemblPlants:AT5G02810.1) - c.1715T>A (EnsemblPlants:AT5G02810.1) Source type: large scale study Cross-references: | |||||||
tmp_5_638843_G_A | 576 | A>V | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.28) Somatic: No Accession: 5:g.638843G>A Codon: GCT/GTT Consequence type: missense Cytogenetic band: Genomic location: 5:g.638843G>A Locations: - p.Ala576Val (EnsemblPlants:AT5G02810.1) - c.1727C>T (EnsemblPlants:AT5G02810.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06911201 | 589 | N>I | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 5:g.638804T>A Codon: AAT/ATT Consequence type: missense Cytogenetic band: Genomic location: 5:g.638804T>A Locations: - p.Asn589Ile (EnsemblPlants:AT5G02810.1) - c.1766A>T (EnsemblPlants:AT5G02810.1) Source type: large scale study Cross-references: | |||||||
ENSVATH03011221 | 592 | N>T | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.45) Somatic: No Accession: 5:g.638795T>G Codon: AAC/ACC Consequence type: missense Cytogenetic band: Genomic location: 5:g.638795T>G Locations: - p.Asn592Thr (EnsemblPlants:AT5G02810.1) - c.1775A>C (EnsemblPlants:AT5G02810.1) Source type: large scale study Cross-references: | |||||||
ENSVATH03011220 | 594 | T>M | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.1) Somatic: No Accession: 5:g.638789G>A Codon: ACG/ATG Consequence type: missense Cytogenetic band: Genomic location: 5:g.638789G>A Locations: - p.Thr594Met (EnsemblPlants:AT5G02810.1) - c.1781C>T (EnsemblPlants:AT5G02810.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06911200 | 601 | T>A | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (1) Somatic: No Accession: 5:g.638769T>C Codon: ACA/GCA Consequence type: missense Cytogenetic band: Genomic location: 5:g.638769T>C Locations: - p.Thr601Ala (EnsemblPlants:AT5G02810.1) - c.1801A>G (EnsemblPlants:AT5G02810.1) Source type: large scale study Cross-references: | |||||||
tmp_5_638689_C_T | 627 | M>I | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.4) Somatic: No Accession: 5:g.638689C>T Codon: ATG/ATA Consequence type: missense Cytogenetic band: Genomic location: 5:g.638689C>T Locations: - p.Met627Ile (EnsemblPlants:AT5G02810.1) - c.1881G>A (EnsemblPlants:AT5G02810.1) Source type: large scale study Cross-references: | |||||||
ENSVATH00602656 | 632 | M>K | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.51) Somatic: No Accession: 5:g.638675A>T Codon: ATG/AAG Consequence type: missense Cytogenetic band: Genomic location: 5:g.638675A>T Locations: - p.Met632Lys (EnsemblPlants:AT5G02810.1) - c.1895T>A (EnsemblPlants:AT5G02810.1) Source type: large scale study Cross-references: | |||||||
ENSVATH13888788 | 657 | S>N | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.09) Somatic: No Accession: 5:g.638600C>T Codon: AGC/AAC Consequence type: missense Cytogenetic band: Genomic location: 5:g.638600C>T Locations: - p.Ser657Asn (EnsemblPlants:AT5G02810.1) - c.1970G>A (EnsemblPlants:AT5G02810.1) Source type: large scale study Cross-references: | |||||||
tmp_5_638558_G_A | 671 | A>V | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.02) Somatic: No Accession: 5:g.638558G>A Codon: GCT/GTT Consequence type: missense Cytogenetic band: Genomic location: 5:g.638558G>A Locations: - p.Ala671Val (EnsemblPlants:AT5G02810.1) - c.2012C>T (EnsemblPlants:AT5G02810.1) Source type: large scale study Cross-references: | |||||||
tmp_5_638507_T_A | 688 | K>M | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 5:g.638507T>A Codon: AAG/ATG Consequence type: missense Cytogenetic band: Genomic location: 5:g.638507T>A Locations: - p.Lys688Met (EnsemblPlants:AT5G02810.1) - c.2063A>T (EnsemblPlants:AT5G02810.1) Source type: large scale study Cross-references: | |||||||
tmp_5_638321_T_G,C | 716 | T>A | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.88) Somatic: No Accession: 5:g.638321T>C Codon: ACT/GCT Consequence type: missense Cytogenetic band: Genomic location: 5:g.638321T>C Locations: - p.Thr716Ala (EnsemblPlants:AT5G02810.1) - c.2146A>G (EnsemblPlants:AT5G02810.1) Source type: large scale study Cross-references: | |||||||
tmp_5_638321_T_G,C | 716 | T>P | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.24) Somatic: No Accession: 5:g.638321T>G Codon: ACT/CCT Consequence type: missense Cytogenetic band: Genomic location: 5:g.638321T>G Locations: - p.Thr716Pro (EnsemblPlants:AT5G02810.1) - c.2146A>C (EnsemblPlants:AT5G02810.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06911193 | 721 | I>R | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated - low confidence (0.1) Somatic: No Accession: 5:g.638305A>C Codon: ATA/AGA Consequence type: missense Cytogenetic band: Genomic location: 5:g.638305A>C Locations: - p.Ile721Arg (EnsemblPlants:AT5G02810.1) - c.2162T>G (EnsemblPlants:AT5G02810.1) Source type: large scale study Cross-references: | |||||||
ENSVATH00602655 | 723 | N>I | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated - low confidence (0.07) Somatic: No Accession: 5:g.638299T>A Codon: AAC/ATC Consequence type: missense Cytogenetic band: Genomic location: 5:g.638299T>A Locations: - p.Asn723Ile (EnsemblPlants:AT5G02810.1) - c.2168A>T (EnsemblPlants:AT5G02810.1) Source type: large scale study Cross-references: | |||||||
tmp_5_638298_G_T | 723 | N>K | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated - low confidence (0.72) Somatic: No Accession: 5:g.638298G>T Codon: AAC/AAA Consequence type: missense Cytogenetic band: Genomic location: 5:g.638298G>T Locations: - p.Asn723Lys (EnsemblPlants:AT5G02810.1) - c.2169C>A (EnsemblPlants:AT5G02810.1) Source type: large scale study Cross-references: | |||||||
tmp_5_638296_A_T | 724 | I>N | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious - low confidence (0.04) Somatic: No Accession: 5:g.638296A>T Codon: ATT/AAT Consequence type: missense Cytogenetic band: Genomic location: 5:g.638296A>T Locations: - p.Ile724Asn (EnsemblPlants:AT5G02810.1) - c.2171T>A (EnsemblPlants:AT5G02810.1) Source type: large scale study Cross-references: | |||||||
ENSVATH13888787 | 725 | E>V | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious - low confidence (0.01) Somatic: No Accession: 5:g.638293T>A Codon: GAG/GTG Consequence type: missense Cytogenetic band: Genomic location: 5:g.638293T>A Locations: - p.Glu725Val (EnsemblPlants:AT5G02810.1) - c.2174A>T (EnsemblPlants:AT5G02810.1) Source type: large scale study Cross-references: | |||||||
tmp_5_638286_G_T | 727 | S>R | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious - low confidence (0) Somatic: No Accession: 5:g.638286G>T Codon: AGC/AGA Consequence type: missense Cytogenetic band: Genomic location: 5:g.638286G>T Locations: - p.Ser727Arg (EnsemblPlants:AT5G02810.1) - c.2181C>A (EnsemblPlants:AT5G02810.1) Source type: large scale study Cross-references: |