Q9SAD3 · SMR8_ARATH
- ProteinCyclin-dependent protein kinase inhibitor SMR8
- GeneSMR8
- StatusUniProtKB reviewed (Swiss-Prot)
- Amino acids110 (go to sequence)
- Protein existenceEvidence at protein level
- Annotation score2/5
Variants
Variant ID(s) | Position(s) | Change | Description | Clinical significance | Provenance | ||
---|---|---|---|---|---|---|---|
ENSVATH10930436 | 18 | S>P | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.23) Somatic: No Accession: 1:g.3550517A>G Codon: TCC/CCC Consequence type: missense Cytogenetic band: Genomic location: 1:g.3550517A>G Locations: - p.Ser18Pro (EnsemblPlants:AT1G10690.1) - c.52T>C (EnsemblPlants:AT1G10690.1) Source type: large scale study Cross-references: | |||||||
ENSVATH00016469 | 54 | Q>H | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.04) Somatic: No Accession: 1:g.3550407C>A Codon: CAG/CAT Consequence type: missense Cytogenetic band: Genomic location: 1:g.3550407C>A Locations: - p.Gln54His (EnsemblPlants:AT1G10690.1) - c.162G>T (EnsemblPlants:AT1G10690.1) Source type: large scale study Cross-references: | |||||||
ENSVATH13876728 | 65 | R>I | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 1:g.3550375C>A Codon: AGA/ATA Consequence type: missense Cytogenetic band: Genomic location: 1:g.3550375C>A Locations: - p.Arg65Ile (EnsemblPlants:AT1G10690.1) - c.194G>T (EnsemblPlants:AT1G10690.1) Source type: large scale study Cross-references: | |||||||
tmp_1_3550363_A_G | 69 | V>A | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.76) Somatic: No Accession: 1:g.3550363A>G Codon: GTC/GCC Consequence type: missense Cytogenetic band: Genomic location: 1:g.3550363A>G Locations: - p.Val69Ala (EnsemblPlants:AT1G10690.1) - c.206T>C (EnsemblPlants:AT1G10690.1) Source type: large scale study Cross-references: | |||||||
tmp_1_3550348_G_C | 74 | A>G | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.01) Somatic: No Accession: 1:g.3550348G>C Codon: GCG/GGG Consequence type: missense Cytogenetic band: Genomic location: 1:g.3550348G>C Locations: - p.Ala74Gly (EnsemblPlants:AT1G10690.1) - c.221C>G (EnsemblPlants:AT1G10690.1) Source type: large scale study Cross-references: | |||||||
tmp_1_3550327_G_A | 81 | P>L | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.19) Somatic: No Accession: 1:g.3550327G>A Codon: CCG/CTG Consequence type: missense Cytogenetic band: Genomic location: 1:g.3550327G>A Locations: - p.Pro81Leu (EnsemblPlants:AT1G10690.1) - c.242C>T (EnsemblPlants:AT1G10690.1) Source type: large scale study Cross-references: | |||||||
ENSVATH00016468 | 87 | Y>N | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.09) Somatic: No Accession: 1:g.3550310A>T Codon: TAC/AAC Consequence type: missense Cytogenetic band: Genomic location: 1:g.3550310A>T Locations: - p.Tyr87Asn (EnsemblPlants:AT1G10690.1) - c.259T>A (EnsemblPlants:AT1G10690.1) Source type: large scale study Cross-references: | |||||||
ENSVATH04552336 | 88 | V>G | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.43) Somatic: No Accession: 1:g.3550306A>C Codon: GTC/GGC Consequence type: missense Cytogenetic band: Genomic location: 1:g.3550306A>C Locations: - p.Val88Gly (EnsemblPlants:AT1G10690.1) - c.263T>G (EnsemblPlants:AT1G10690.1) Source type: large scale study Cross-references: | |||||||
tmp_1_3550282_G_T | 96 | S>Y | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.01) Somatic: No Accession: 1:g.3550282G>T Codon: TCT/TAT Consequence type: missense Cytogenetic band: Genomic location: 1:g.3550282G>T Locations: - p.Ser96Tyr (EnsemblPlants:AT1G10690.1) - c.287C>A (EnsemblPlants:AT1G10690.1) Source type: large scale study Cross-references: |