Q8L860 · TOL9_ARATH
- ProteinTOM1-like protein 9
- GeneTOL9
- StatusUniProtKB reviewed (Swiss-Prot)
- Amino acids675 (go to sequence)
- Protein existenceEvidence at protein level
- Annotation score4/5
Variants
Variant ID(s) | Position(s) | Change | Description | Clinical significance | Provenance | ||
---|---|---|---|---|---|---|---|
ENSVATH14328150 | 11 | S>N | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.04) Somatic: No Accession: 4:g.15799407G>A Codon: AGC/AAC Consequence type: missense Cytogenetic band: Genomic location: 4:g.15799407G>A Locations: - p.Ser11Asn (EnsemblPlants:AT4G32760.1) - c.32G>A (EnsemblPlants:AT4G32760.1) Source type: large scale study Cross-references: | |||||||
ENSVATH14328151 | 28 | M>I | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (1) Somatic: No Accession: 4:g.15799459G>T Codon: ATG/ATT Consequence type: missense Cytogenetic band: Genomic location: 4:g.15799459G>T Locations: - p.Met28Ile (EnsemblPlants:AT4G32760.1) - c.84G>T (EnsemblPlants:AT4G32760.1) Source type: large scale study Cross-references: | |||||||
tmp_4_15800782_C_A | 132 | R>S | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 4:g.15800782C>A Codon: CGT/AGT Consequence type: missense Cytogenetic band: Genomic location: 4:g.15800782C>A Locations: - p.Arg132Ser (EnsemblPlants:AT4G32760.1) - c.394C>A (EnsemblPlants:AT4G32760.1) Source type: large scale study Cross-references: | |||||||
tmp_4_15800893_G_T | 169 | G>C | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.04) Somatic: No Accession: 4:g.15800893G>T Codon: GGT/TGT Consequence type: missense Cytogenetic band: Genomic location: 4:g.15800893G>T Locations: - p.Gly169Cys (EnsemblPlants:AT4G32760.1) - c.505G>T (EnsemblPlants:AT4G32760.1) Source type: large scale study Cross-references: | |||||||
tmp_4_15800903_T_C | 172 | V>A | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (1) Somatic: No Accession: 4:g.15800903T>C Codon: GTG/GCG Consequence type: missense Cytogenetic band: Genomic location: 4:g.15800903T>C Locations: - p.Val172Ala (EnsemblPlants:AT4G32760.1) - c.515T>C (EnsemblPlants:AT4G32760.1) Source type: large scale study Cross-references: | |||||||
ENSVATH12355829 | 193 | K>R | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (1) Somatic: No Accession: 4:g.15801399A>G Codon: AAA/AGA Consequence type: missense Cytogenetic band: Genomic location: 4:g.15801399A>G Locations: - p.Lys193Arg (EnsemblPlants:AT4G32760.1) - c.578A>G (EnsemblPlants:AT4G32760.1) Source type: large scale study Cross-references: | |||||||
tmp_4_15802045_G_T | 251 | A>S | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.28) Somatic: No Accession: 4:g.15802045G>T Codon: GCT/TCT Consequence type: missense Cytogenetic band: Genomic location: 4:g.15802045G>T Locations: - p.Ala251Ser (EnsemblPlants:AT4G32760.1) - c.751G>T (EnsemblPlants:AT4G32760.1) Source type: large scale study Cross-references: | |||||||
tmp_4_15802157_T_G | 288 | L>R | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 4:g.15802157T>G Codon: CTT/CGT Consequence type: missense Cytogenetic band: Genomic location: 4:g.15802157T>G Locations: - p.Leu288Arg (EnsemblPlants:AT4G32760.1) - c.863T>G (EnsemblPlants:AT4G32760.1) Source type: large scale study Cross-references: | |||||||
tmp_4_15802542_C_T | 310 | S>L | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.06) Somatic: No Accession: 4:g.15802542C>T Codon: TCG/TTG Consequence type: missense Cytogenetic band: Genomic location: 4:g.15802542C>T Locations: - p.Ser310Leu (EnsemblPlants:AT4G32760.1) - c.929C>T (EnsemblPlants:AT4G32760.1) Source type: large scale study Cross-references: | |||||||
tmp_4_15802544_A_C | 311 | S>R | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.04) Somatic: No Accession: 4:g.15802544A>C Codon: AGC/CGC Consequence type: missense Cytogenetic band: Genomic location: 4:g.15802544A>C Locations: - p.Ser311Arg (EnsemblPlants:AT4G32760.1) - c.931A>C (EnsemblPlants:AT4G32760.1) Source type: large scale study Cross-references: | |||||||
ENSVATH12355832 | 314 | N>K | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.94) Somatic: No Accession: 4:g.15802555C>A Codon: AAC/AAA Consequence type: missense Cytogenetic band: Genomic location: 4:g.15802555C>A Locations: - p.Asn314Lys (EnsemblPlants:AT4G32760.1) - c.942C>A (EnsemblPlants:AT4G32760.1) Source type: large scale study Cross-references: | |||||||
ENSVATH02951657 | 332 | A>V | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.35) Somatic: No Accession: 4:g.15802608C>T Codon: GCC/GTC Consequence type: missense Cytogenetic band: Genomic location: 4:g.15802608C>T Locations: - p.Ala332Val (EnsemblPlants:AT4G32760.1) - c.995C>T (EnsemblPlants:AT4G32760.1) Source type: large scale study Cross-references: | |||||||
tmp_4_15802659_T_G | 349 | V>G | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 4:g.15802659T>G Codon: GTT/GGT Consequence type: missense Cytogenetic band: Genomic location: 4:g.15802659T>G Locations: - p.Val349Gly (EnsemblPlants:AT4G32760.1) - c.1046T>G (EnsemblPlants:AT4G32760.1) Source type: large scale study Cross-references: | |||||||
ENSVATH12355833 | 354 | P>S | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.18) Somatic: No Accession: 4:g.15802673C>T Codon: CCA/TCA Consequence type: missense Cytogenetic band: Genomic location: 4:g.15802673C>T Locations: - p.Pro354Ser (EnsemblPlants:AT4G32760.1) - c.1060C>T (EnsemblPlants:AT4G32760.1) Source type: large scale study Cross-references: | |||||||
tmp_4_15802746_C_A | 378 | P>Q | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.51) Somatic: No Accession: 4:g.15802746C>A Codon: CCA/CAA Consequence type: missense Cytogenetic band: Genomic location: 4:g.15802746C>A Locations: - p.Pro378Gln (EnsemblPlants:AT4G32760.1) - c.1133C>A (EnsemblPlants:AT4G32760.1) Source type: large scale study Cross-references: | |||||||
ENSVATH00549036 | 443 | P>L | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.68) Somatic: No Accession: 4:g.15802941C>T Codon: CCT/CTT Consequence type: missense Cytogenetic band: Genomic location: 4:g.15802941C>T Locations: - p.Pro443Leu (EnsemblPlants:AT4G32760.1) - c.1328C>T (EnsemblPlants:AT4G32760.1) Source type: large scale study Cross-references: | |||||||
ENSVATH00549037 | 446 | Q>E | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.02) Somatic: No Accession: 4:g.15802949C>G Codon: CAA/GAA Consequence type: missense Cytogenetic band: Genomic location: 4:g.15802949C>G Locations: - p.Gln446Glu (EnsemblPlants:AT4G32760.1) - c.1336C>G (EnsemblPlants:AT4G32760.1) Source type: large scale study Cross-references: | |||||||
tmp_4_15802960_G_C | 449 | Q>H | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.08) Somatic: No Accession: 4:g.15802960G>C Codon: CAG/CAC Consequence type: missense Cytogenetic band: Genomic location: 4:g.15802960G>C Locations: - p.Gln449His (EnsemblPlants:AT4G32760.1) - c.1347G>C (EnsemblPlants:AT4G32760.1) Source type: large scale study Cross-references: | |||||||
ENSVATH14328180 | 454 | A>T | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.56) Somatic: No Accession: 4:g.15803164G>A Codon: GCC/ACC Consequence type: missense Cytogenetic band: Genomic location: 4:g.15803164G>A Locations: - p.Ala454Thr (EnsemblPlants:AT4G32760.1) - c.1360G>A (EnsemblPlants:AT4G32760.1) Source type: large scale study Cross-references: | |||||||
ENSVATH00549039 | 467 | A>T | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.32) Somatic: No Accession: 4:g.15803203G>A Codon: GCT/ACT Consequence type: missense Cytogenetic band: Genomic location: 4:g.15803203G>A Locations: - p.Ala467Thr (EnsemblPlants:AT4G32760.1) - c.1399G>A (EnsemblPlants:AT4G32760.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06814052 | 489 | T>N | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.44) Somatic: No Accession: 4:g.15803270C>A Codon: ACT/AAT Consequence type: missense Cytogenetic band: Genomic location: 4:g.15803270C>A Locations: - p.Thr489Asn (EnsemblPlants:AT4G32760.1) - c.1466C>A (EnsemblPlants:AT4G32760.1) Source type: large scale study Cross-references: | |||||||
ENSVATH00549043 | 513 | P>Q | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.75) Somatic: No Accession: 4:g.15803342C>A Codon: CCA/CAA Consequence type: missense Cytogenetic band: Genomic location: 4:g.15803342C>A Locations: - p.Pro513Gln (EnsemblPlants:AT4G32760.1) - c.1538C>A (EnsemblPlants:AT4G32760.1) Source type: large scale study Cross-references: | |||||||
ENSVATH00549045 | 534 | I>N | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.28) Somatic: No Accession: 4:g.15803405T>A Codon: ATC/AAC Consequence type: missense Cytogenetic band: Genomic location: 4:g.15803405T>A Locations: - p.Ile534Asn (EnsemblPlants:AT4G32760.1) - c.1601T>A (EnsemblPlants:AT4G32760.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06814054 | 534 | I>V | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.54) Somatic: No Accession: 4:g.15803404A>G Codon: ATC/GTC Consequence type: missense Cytogenetic band: Genomic location: 4:g.15803404A>G Locations: - p.Ile534Val (EnsemblPlants:AT4G32760.1) - c.1600A>G (EnsemblPlants:AT4G32760.1) Source type: large scale study Cross-references: | |||||||
tmp_4_15803432_A_C | 543 | N>T | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.54) Somatic: No Accession: 4:g.15803432A>C Codon: AAC/ACC Consequence type: missense Cytogenetic band: Genomic location: 4:g.15803432A>C Locations: - p.Asn543Thr (EnsemblPlants:AT4G32760.1) - c.1628A>C (EnsemblPlants:AT4G32760.1) Source type: large scale study Cross-references: | |||||||
ENSVATH06814055 | 554 | A>T | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.66) Somatic: No Accession: 4:g.15803464G>A Codon: GCT/ACT Consequence type: missense Cytogenetic band: Genomic location: 4:g.15803464G>A Locations: - p.Ala554Thr (EnsemblPlants:AT4G32760.1) - c.1660G>A (EnsemblPlants:AT4G32760.1) Source type: large scale study Cross-references: | |||||||
ENSVATH00549046 | 555 | L>F | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.65) Somatic: No Accession: 4:g.15803467C>T Codon: CTT/TTT Consequence type: missense Cytogenetic band: Genomic location: 4:g.15803467C>T Locations: - p.Leu555Phe (EnsemblPlants:AT4G32760.1) - c.1663C>T (EnsemblPlants:AT4G32760.1) Source type: large scale study Cross-references: | |||||||
ENSVATH00549046 | 555 | L>I | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.48) Somatic: No Accession: 4:g.15803467C>A Codon: CTT/ATT Consequence type: missense Cytogenetic band: Genomic location: 4:g.15803467C>A Locations: - p.Leu555Ile (EnsemblPlants:AT4G32760.1) - c.1663C>A (EnsemblPlants:AT4G32760.1) Source type: large scale study Cross-references: | |||||||
tmp_4_15803483_A_C,T | 560 | Q>L | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.65) Somatic: No Accession: 4:g.15803483A>T Codon: CAA/CTA Consequence type: missense Cytogenetic band: Genomic location: 4:g.15803483A>T Locations: - p.Gln560Leu (EnsemblPlants:AT4G32760.1) - c.1679A>T (EnsemblPlants:AT4G32760.1) Source type: large scale study Cross-references: | |||||||
tmp_4_15803483_A_C,T | 560 | Q>P | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.25) Somatic: No Accession: 4:g.15803483A>C Codon: CAA/CCA Consequence type: missense Cytogenetic band: Genomic location: 4:g.15803483A>C Locations: - p.Gln560Pro (EnsemblPlants:AT4G32760.1) - c.1679A>C (EnsemblPlants:AT4G32760.1) Source type: large scale study Cross-references: | |||||||
tmp_4_15803541_A_C | 579 | Q>H | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.59) Somatic: No Accession: 4:g.15803541A>C Codon: CAA/CAC Consequence type: missense Cytogenetic band: Genomic location: 4:g.15803541A>C Locations: - p.Gln579His (EnsemblPlants:AT4G32760.1) - c.1737A>C (EnsemblPlants:AT4G32760.1) Source type: large scale study Cross-references: | |||||||
tmp_4_15803672_A_G | 623 | D>G | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.06) Somatic: No Accession: 4:g.15803672A>G Codon: GAC/GGC Consequence type: missense Cytogenetic band: Genomic location: 4:g.15803672A>G Locations: - p.Asp623Gly (EnsemblPlants:AT4G32760.1) - c.1868A>G (EnsemblPlants:AT4G32760.1) Source type: large scale study Cross-references: | |||||||
tmp_4_15803681_C_T | 626 | S>L | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.68) Somatic: No Accession: 4:g.15803681C>T Codon: TCG/TTG Consequence type: missense Cytogenetic band: Genomic location: 4:g.15803681C>T Locations: - p.Ser626Leu (EnsemblPlants:AT4G32760.1) - c.1877C>T (EnsemblPlants:AT4G32760.1) Source type: large scale study Cross-references: | |||||||
tmp_4_15803689_G_A | 629 | V>I | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.22) Somatic: No Accession: 4:g.15803689G>A Codon: GTA/ATA Consequence type: missense Cytogenetic band: Genomic location: 4:g.15803689G>A Locations: - p.Val629Ile (EnsemblPlants:AT4G32760.1) - c.1885G>A (EnsemblPlants:AT4G32760.1) Source type: large scale study Cross-references: | |||||||
ENSVATH00549047 | 630 | A>P | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.39) Somatic: No Accession: 4:g.15803692G>C Codon: GCA/CCA Consequence type: missense Cytogenetic band: Genomic location: 4:g.15803692G>C Locations: - p.Ala630Pro (EnsemblPlants:AT4G32760.1) - c.1888G>C (EnsemblPlants:AT4G32760.1) Source type: large scale study Cross-references: | |||||||
ENSVATH14328182 | 639 | L>R | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.39) Somatic: No Accession: 4:g.15803720T>G Codon: CTG/CGG Consequence type: missense Cytogenetic band: Genomic location: 4:g.15803720T>G Locations: - p.Leu639Arg (EnsemblPlants:AT4G32760.1) - c.1916T>G (EnsemblPlants:AT4G32760.1) Source type: large scale study Cross-references: | |||||||
tmp_4_15803728_A_G | 642 | M>V | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.41) Somatic: No Accession: 4:g.15803728A>G Codon: ATG/GTG Consequence type: missense Cytogenetic band: Genomic location: 4:g.15803728A>G Locations: - p.Met642Val (EnsemblPlants:AT4G32760.1) - c.1924A>G (EnsemblPlants:AT4G32760.1) Source type: large scale study Cross-references: | |||||||
tmp_4_15803829_G_T | 675 | M>I | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.06) Somatic: No Accession: 4:g.15803829G>T Codon: ATG/ATT Consequence type: missense Cytogenetic band: Genomic location: 4:g.15803829G>T Locations: - p.Met675Ile (EnsemblPlants:AT4G32760.1) - c.2025G>T (EnsemblPlants:AT4G32760.1) Source type: large scale study Cross-references: |