A0A1P8ASU8 · A0A1P8ASU8_ARATH
- ProteinCyclin-dependent kinase inhibitor
- GeneICK5
- StatusUniProtKB unreviewed (TrEMBL)
- Amino acids200 (go to sequence)
- Protein existenceInferred from homology
- Annotation score2/5
Variants
Variant ID(s) | Position(s) | Change | Description | Clinical significance | Provenance | ||
---|---|---|---|---|---|---|---|
ENSVATH01330016 | 11 | P>S | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated - low confidence (0.95) Somatic: No Accession: 1:g.18366544G>A Codon: CCC/TCC Consequence type: missense Cytogenetic band: Genomic location: 1:g.18366544G>A Locations: - p.Pro11Ser (EnsemblPlants:AT1G49620.3) - c.31C>T (EnsemblPlants:AT1G49620.3) Source type: large scale study Cross-references: | |||||||
ENSVATH01330015 | 15 | S>F | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious - low confidence (0.01) Somatic: No Accession: 1:g.18366531G>A Codon: TCT/TTT Consequence type: missense Cytogenetic band: Genomic location: 1:g.18366531G>A Locations: - p.Ser15Phe (EnsemblPlants:AT1G49620.3) - c.44C>T (EnsemblPlants:AT1G49620.3) Source type: large scale study Cross-references: | |||||||
ENSVATH01330015 | 15 | S>Y | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious - low confidence (0.01) Somatic: No Accession: 1:g.18366531G>T Codon: TCT/TAT Consequence type: missense Cytogenetic band: Genomic location: 1:g.18366531G>T Locations: - p.Ser15Tyr (EnsemblPlants:AT1G49620.3) - c.44C>A (EnsemblPlants:AT1G49620.3) Source type: large scale study Cross-references: | |||||||
ENSVATH01330014 | 21 | N>D | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated - low confidence (0.14) Somatic: No Accession: 1:g.18366514T>C Codon: AAC/GAC Consequence type: missense Cytogenetic band: Genomic location: 1:g.18366514T>C Locations: - p.Asn21Asp (EnsemblPlants:AT1G49620.3) - c.61A>G (EnsemblPlants:AT1G49620.3) Source type: large scale study Cross-references: | |||||||
tmp_1_18366478_C_T | 33 | V>I | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.52) Somatic: No Accession: 1:g.18366478C>T Codon: GTT/ATT Consequence type: missense Cytogenetic band: Genomic location: 1:g.18366478C>T Locations: - p.Val33Ile (EnsemblPlants:AT1G49620.3) - c.97G>A (EnsemblPlants:AT1G49620.3) Source type: large scale study Cross-references: | |||||||
ENSVATH13466902 | 40 | T>N | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.12) Somatic: No Accession: 1:g.18366456G>T Codon: ACT/AAT Consequence type: missense Cytogenetic band: Genomic location: 1:g.18366456G>T Locations: - p.Thr40Asn (EnsemblPlants:AT1G49620.3) - c.119C>A (EnsemblPlants:AT1G49620.3) Source type: large scale study Cross-references: | |||||||
tmp_1_18366454_G_A | 41 | L>F | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.14) Somatic: No Accession: 1:g.18366454G>A Codon: CTT/TTT Consequence type: missense Cytogenetic band: Genomic location: 1:g.18366454G>A Locations: - p.Leu41Phe (EnsemblPlants:AT1G49620.3) - c.121C>T (EnsemblPlants:AT1G49620.3) Source type: large scale study Cross-references: | |||||||
ENSVATH04916502 | 56 | S>F | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.01) Somatic: No Accession: 1:g.18366408G>A Codon: TCC/TTC Consequence type: missense Cytogenetic band: Genomic location: 1:g.18366408G>A Locations: - p.Ser56Phe (EnsemblPlants:AT1G49620.3) - c.167C>T (EnsemblPlants:AT1G49620.3) Source type: large scale study Cross-references: | |||||||
ENSVATH14271646 | 57 | G>R | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.03) Somatic: No Accession: 1:g.18366406C>T Codon: GGA/AGA Consequence type: missense Cytogenetic band: Genomic location: 1:g.18366406C>T Locations: - p.Gly57Arg (EnsemblPlants:AT1G49620.3) - c.169G>A (EnsemblPlants:AT1G49620.3) Source type: large scale study Cross-references: | |||||||
tmp_1_18366396_C_T | 60 | C>Y | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.31) Somatic: No Accession: 1:g.18366396C>T Codon: TGC/TAC Consequence type: missense Cytogenetic band: Genomic location: 1:g.18366396C>T Locations: - p.Cys60Tyr (EnsemblPlants:AT1G49620.3) - c.179G>A (EnsemblPlants:AT1G49620.3) Source type: large scale study Cross-references: | |||||||
ENSVATH14271645 | 63 | A>S | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.76) Somatic: No Accession: 1:g.18366388C>A Codon: GCG/TCG Consequence type: missense Cytogenetic band: Genomic location: 1:g.18366388C>A Locations: - p.Ala63Ser (EnsemblPlants:AT1G49620.3) - c.187G>T (EnsemblPlants:AT1G49620.3) Source type: large scale study Cross-references: | |||||||
ENSVATH13466901 | 66 | E>D | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.66) Somatic: No Accession: 1:g.18366377T>A Codon: GAA/GAT Consequence type: missense Cytogenetic band: Genomic location: 1:g.18366377T>A Locations: - p.Glu66Asp (EnsemblPlants:AT1G49620.3) - c.198A>T (EnsemblPlants:AT1G49620.3) Source type: large scale study Cross-references: | |||||||
ENSVATH04916499 | 70 | D>V | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.01) Somatic: No Accession: 1:g.18366366T>A Codon: GAT/GTT Consequence type: missense Cytogenetic band: Genomic location: 1:g.18366366T>A Locations: - p.Asp70Val (EnsemblPlants:AT1G49620.3) - c.209A>T (EnsemblPlants:AT1G49620.3) Source type: large scale study Cross-references: | |||||||
tmp_1_18366363_T_C | 71 | H>R | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.16) Somatic: No Accession: 1:g.18366363T>C Codon: CAT/CGT Consequence type: missense Cytogenetic band: Genomic location: 1:g.18366363T>C Locations: - p.His71Arg (EnsemblPlants:AT1G49620.3) - c.212A>G (EnsemblPlants:AT1G49620.3) Source type: large scale study Cross-references: | |||||||
ENSVATH00089958 | 72 | L>R | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.5) Somatic: No Accession: 1:g.18366360A>C Codon: CTA/CGA Consequence type: missense Cytogenetic band: Genomic location: 1:g.18366360A>C Locations: - p.Leu72Arg (EnsemblPlants:AT1G49620.3) - c.215T>G (EnsemblPlants:AT1G49620.3) Source type: large scale study Cross-references: | |||||||
ENSVATH00089957 | 76 | I>V | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.89) Somatic: No Accession: 1:g.18366349T>C Codon: ATC/GTC Consequence type: missense Cytogenetic band: Genomic location: 1:g.18366349T>C Locations: - p.Ile76Val (EnsemblPlants:AT1G49620.3) - c.226A>G (EnsemblPlants:AT1G49620.3) Source type: large scale study Cross-references: | |||||||
ENSVATH13466900 | 83 | S>T | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.36) Somatic: No Accession: 1:g.18366327C>G Codon: AGC/ACC Consequence type: missense Cytogenetic band: Genomic location: 1:g.18366327C>G Locations: - p.Ser83Thr (EnsemblPlants:AT1G49620.3) - c.248G>C (EnsemblPlants:AT1G49620.3) Source type: large scale study Cross-references: | |||||||
ENSVATH01330012 | 90 | T>S | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.69) Somatic: No Accession: 1:g.18366306G>C Codon: ACT/AGT Consequence type: missense Cytogenetic band: Genomic location: 1:g.18366306G>C Locations: - p.Thr90Ser (EnsemblPlants:AT1G49620.3) - c.269C>G (EnsemblPlants:AT1G49620.3) Source type: large scale study Cross-references: | |||||||
tmp_1_18366282_T_G | 98 | E>A | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.01) Somatic: No Accession: 1:g.18366282T>G Codon: GAG/GCG Consequence type: missense Cytogenetic band: Genomic location: 1:g.18366282T>G Locations: - p.Glu98Ala (EnsemblPlants:AT1G49620.3) - c.293A>C (EnsemblPlants:AT1G49620.3) Source type: large scale study Cross-references: | |||||||
tmp_1_18366161_G_C | 99 | A>G | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.24) Somatic: No Accession: 1:g.18366161G>C Codon: GCT/GGT Consequence type: missense Cytogenetic band: Genomic location: 1:g.18366161G>C Locations: - p.Ala99Gly (EnsemblPlants:AT1G49620.3) - c.296C>G (EnsemblPlants:AT1G49620.3) Source type: large scale study Cross-references: | |||||||
tmp_1_18366159_G_T,A | 100 | H>N | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.36) Somatic: No Accession: 1:g.18366159G>T Codon: CAT/AAT Consequence type: missense Cytogenetic band: Genomic location: 1:g.18366159G>T Locations: - p.His100Asn (EnsemblPlants:AT1G49620.3) - c.298C>A (EnsemblPlants:AT1G49620.3) Source type: large scale study Cross-references: | |||||||
tmp_1_18366159_G_T,A | 100 | H>Y | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.03) Somatic: No Accession: 1:g.18366159G>A Codon: CAT/TAT Consequence type: missense Cytogenetic band: Genomic location: 1:g.18366159G>A Locations: - p.His100Tyr (EnsemblPlants:AT1G49620.3) - c.298C>T (EnsemblPlants:AT1G49620.3) Source type: large scale study Cross-references: | |||||||
tmp_1_18366156_C_T | 101 | E>K | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.62) Somatic: No Accession: 1:g.18366156C>T Codon: GAA/AAA Consequence type: missense Cytogenetic band: Genomic location: 1:g.18366156C>T Locations: - p.Glu101Lys (EnsemblPlants:AT1G49620.3) - c.301G>A (EnsemblPlants:AT1G49620.3) Source type: large scale study Cross-references: | |||||||
ENSVATH13466898 | 106 | E>K | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.02) Somatic: No Accession: 1:g.18366141C>T Codon: GAA/AAA Consequence type: missense Cytogenetic band: Genomic location: 1:g.18366141C>T Locations: - p.Glu106Lys (EnsemblPlants:AT1G49620.3) - c.316G>A (EnsemblPlants:AT1G49620.3) Source type: large scale study Cross-references: | |||||||
tmp_1_18365996_G_T | 126 | L>M | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.23) Somatic: No Accession: 1:g.18365996G>T Codon: CTG/ATG Consequence type: missense Cytogenetic band: Genomic location: 1:g.18365996G>T Locations: - p.Leu126Met (EnsemblPlants:AT1G49620.3) - c.376C>A (EnsemblPlants:AT1G49620.3) Source type: large scale study Cross-references: | |||||||
ENSVATH13466895 | 134 | S>L | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 1:g.18365971G>A Codon: TCG/TTG Consequence type: missense Cytogenetic band: Genomic location: 1:g.18365971G>A Locations: - p.Ser134Leu (EnsemblPlants:AT1G49620.3) - c.401C>T (EnsemblPlants:AT1G49620.3) Source type: large scale study Cross-references: | |||||||
ENSVATH01330002 | 139 | M>R | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.53) Somatic: No Accession: 1:g.18365956A>C Codon: ATG/AGG Consequence type: missense Cytogenetic band: Genomic location: 1:g.18365956A>C Locations: - p.Met139Arg (EnsemblPlants:AT1G49620.3) - c.416T>G (EnsemblPlants:AT1G49620.3) Source type: large scale study Cross-references: | |||||||
tmp_1_18365944_C_T | 143 | R>K | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.4) Somatic: No Accession: 1:g.18365944C>T Codon: AGA/AAA Consequence type: missense Cytogenetic band: Genomic location: 1:g.18365944C>T Locations: - p.Arg143Lys (EnsemblPlants:AT1G49620.3) - c.428G>A (EnsemblPlants:AT1G49620.3) Source type: large scale study Cross-references: | |||||||
ENSVATH04916488 | 145 | T>M | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.27) Somatic: No Accession: 1:g.18365938G>A Codon: ACG/ATG Consequence type: missense Cytogenetic band: Genomic location: 1:g.18365938G>A Locations: - p.Thr145Met (EnsemblPlants:AT1G49620.3) - c.434C>T (EnsemblPlants:AT1G49620.3) Source type: large scale study Cross-references: | |||||||
ENSVATH04916487 | 149 | K>T | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.56) Somatic: No Accession: 1:g.18365926T>G Codon: AAG/ACG Consequence type: missense Cytogenetic band: Genomic location: 1:g.18365926T>G Locations: - p.Lys149Thr (EnsemblPlants:AT1G49620.3) - c.446A>C (EnsemblPlants:AT1G49620.3) Source type: large scale study Cross-references: | |||||||
ENSVATH14271593 | 162 | D>N | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.03) Somatic: No Accession: 1:g.18365888C>T Codon: GAC/AAC Consequence type: missense Cytogenetic band: Genomic location: 1:g.18365888C>T Locations: - p.Asp162Asn (EnsemblPlants:AT1G49620.3) - c.484G>A (EnsemblPlants:AT1G49620.3) Source type: large scale study Cross-references: | |||||||
ENSVATH01330000 | 166 | A>T | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.32) Somatic: No Accession: 1:g.18365876C>T Codon: GCG/ACG Consequence type: missense Cytogenetic band: Genomic location: 1:g.18365876C>T Locations: - p.Ala166Thr (EnsemblPlants:AT1G49620.3) - c.496G>A (EnsemblPlants:AT1G49620.3) Source type: large scale study Cross-references: | |||||||
ENSVATH00089954 | 170 | Y>H | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.53) Somatic: No Accession: 1:g.18365864A>G Codon: TAC/CAC Consequence type: missense Cytogenetic band: Genomic location: 1:g.18365864A>G Locations: - p.Tyr170His (EnsemblPlants:AT1G49620.3) - c.508T>C (EnsemblPlants:AT1G49620.3) Source type: large scale study Cross-references: |