Q93YU5 · SEC8_ARATH
- ProteinExocyst complex component SEC8
- GeneSEC8
- StatusUniProtKB reviewed (Swiss-Prot)
- Amino acids1053 (go to sequence)
- Protein existenceEvidence at protein level
- Annotation score5/5
Variants
Variant ID(s) | Position(s) | Change | Description | Clinical significance | Provenance | ||
---|---|---|---|---|---|---|---|
ENSVATH05803617 | 114 | R>H | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.06) Somatic: No Accession: 3:g.3227422C>T Codon: CGC/CAC Consequence type: missense Cytogenetic band: Genomic location: 3:g.3227422C>T Locations: - p.Arg114His (EnsemblPlants:AT3G10380.1) - c.341G>A (EnsemblPlants:AT3G10380.1) Source type: large scale study Cross-references: | |||||||
tmp_3_3227083_C_A | 149 | E>D | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.01) Somatic: No Accession: 3:g.3227083C>A Codon: GAG/GAT Consequence type: missense Cytogenetic band: Genomic location: 3:g.3227083C>A Locations: - p.Glu149Asp (EnsemblPlants:AT3G10380.1) - c.447G>T (EnsemblPlants:AT3G10380.1) Source type: large scale study Cross-references: | |||||||
tmp_3_3226729_C_T | 193 | R>Q | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.07) Somatic: No Accession: 3:g.3226729C>T Codon: CGG/CAG Consequence type: missense Cytogenetic band: Genomic location: 3:g.3226729C>T Locations: - p.Arg193Gln (EnsemblPlants:AT3G10380.1) - c.578G>A (EnsemblPlants:AT3G10380.1) Source type: large scale study Cross-references: | |||||||
tmp_3_3226381_T_G | 260 | R>S | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.94) Somatic: No Accession: 3:g.3226381T>G Codon: AGA/AGC Consequence type: missense Cytogenetic band: Genomic location: 3:g.3226381T>G Locations: - p.Arg260Ser (EnsemblPlants:AT3G10380.1) - c.780A>C (EnsemblPlants:AT3G10380.1) Source type: large scale study Cross-references: | |||||||
tmp_3_3226352_G_C | 270 | A>G | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.64) Somatic: No Accession: 3:g.3226352G>C Codon: GCT/GGT Consequence type: missense Cytogenetic band: Genomic location: 3:g.3226352G>C Locations: - p.Ala270Gly (EnsemblPlants:AT3G10380.1) - c.809C>G (EnsemblPlants:AT3G10380.1) Source type: large scale study Cross-references: | |||||||
tmp_3_3225910_C_A | 287 | V>L | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (1) Somatic: No Accession: 3:g.3225910C>A Codon: GTA/TTA Consequence type: missense Cytogenetic band: Genomic location: 3:g.3225910C>A Locations: - p.Val287Leu (EnsemblPlants:AT3G10380.1) - c.859G>T (EnsemblPlants:AT3G10380.1) Source type: large scale study Cross-references: | |||||||
tmp_3_3225879_G_A | 297 | A>V | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.26) Somatic: No Accession: 3:g.3225879G>A Codon: GCC/GTC Consequence type: missense Cytogenetic band: Genomic location: 3:g.3225879G>A Locations: - p.Ala297Val (EnsemblPlants:AT3G10380.1) - c.890C>T (EnsemblPlants:AT3G10380.1) Source type: large scale study Cross-references: | |||||||
ENSVATH13892758 | 301 | T>A | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.79) Somatic: No Accession: 3:g.3225868T>C Codon: ACT/GCT Consequence type: missense Cytogenetic band: Genomic location: 3:g.3225868T>C Locations: - p.Thr301Ala (EnsemblPlants:AT3G10380.1) - c.901A>G (EnsemblPlants:AT3G10380.1) Source type: large scale study Cross-references: | |||||||
tmp_3_3225633_C_A | 352 | A>S | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.07) Somatic: No Accession: 3:g.3225633C>A Codon: GCA/TCA Consequence type: missense Cytogenetic band: Genomic location: 3:g.3225633C>A Locations: - p.Ala352Ser (EnsemblPlants:AT3G10380.1) - c.1054G>T (EnsemblPlants:AT3G10380.1) Source type: large scale study Cross-references: | |||||||
ENSVATH05803597 | 387 | A>T | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.56) Somatic: No Accession: 3:g.3225188C>T Codon: GCG/ACG Consequence type: missense Cytogenetic band: Genomic location: 3:g.3225188C>T Locations: - p.Ala387Thr (EnsemblPlants:AT3G10380.1) - c.1159G>A (EnsemblPlants:AT3G10380.1) Source type: large scale study Cross-references: | |||||||
ENSVATH00315127 | 394 | S>N | Plants were checked bi-weekly for presence of first buds and the average flowering time of 4 plants of the same accession were collected [16c and 16 hrs daylight] (EnsemblGenome) | 1000Genomes | |||
Consequence: missense Predictions: - SIFT: tolerated (0.38) Somatic: No Accession: 3:g.3225166C>T Codon: AGT/AAT Consequence type: missense Cytogenetic band: Genomic location: 3:g.3225166C>T Locations: - p.Ser394Asn (EnsemblPlants:AT3G10380.1) - c.1181G>A (EnsemblPlants:AT3G10380.1) Source type: large scale study Cross-references: | |||||||
ENSVATH00315126 | 397 | A>T | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.45) Somatic: No Accession: 3:g.3225158C>T Codon: GCT/ACT Consequence type: missense Cytogenetic band: Genomic location: 3:g.3225158C>T Locations: - p.Ala397Thr (EnsemblPlants:AT3G10380.1) - c.1189G>A (EnsemblPlants:AT3G10380.1) Source type: large scale study Cross-references: | |||||||
ENSVATH00315125 | 408 | A>V | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.49) Somatic: No Accession: 3:g.3225124G>A Codon: GCC/GTC Consequence type: missense Cytogenetic band: Genomic location: 3:g.3225124G>A Locations: - p.Ala408Val (EnsemblPlants:AT3G10380.1) - c.1223C>T (EnsemblPlants:AT3G10380.1) Source type: large scale study Cross-references: | |||||||
tmp_3_3225118_C_T | 410 | R>Q | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (1) Somatic: No Accession: 3:g.3225118C>T Codon: CGG/CAG Consequence type: missense Cytogenetic band: Genomic location: 3:g.3225118C>T Locations: - p.Arg410Gln (EnsemblPlants:AT3G10380.1) - c.1229G>A (EnsemblPlants:AT3G10380.1) Source type: large scale study Cross-references: | |||||||
tmp_3_3225074_T_A | 425 | T>S | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.3) Somatic: No Accession: 3:g.3225074T>A Codon: ACT/TCT Consequence type: missense Cytogenetic band: Genomic location: 3:g.3225074T>A Locations: - p.Thr425Ser (EnsemblPlants:AT3G10380.1) - c.1273A>T (EnsemblPlants:AT3G10380.1) Source type: large scale study Cross-references: | |||||||
ENSVATH05803590 | 500 | Q>R | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.34) Somatic: No Accession: 3:g.3224763T>C Codon: CAA/CGA Consequence type: missense Cytogenetic band: Genomic location: 3:g.3224763T>C Locations: - p.Gln500Arg (EnsemblPlants:AT3G10380.1) - c.1499A>G (EnsemblPlants:AT3G10380.1) Source type: large scale study Cross-references: | |||||||
tmp_3_3224560_G_A | 535 | A>V | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.13) Somatic: No Accession: 3:g.3224560G>A Codon: GCA/GTA Consequence type: missense Cytogenetic band: Genomic location: 3:g.3224560G>A Locations: - p.Ala535Val (EnsemblPlants:AT3G10380.1) - c.1604C>T (EnsemblPlants:AT3G10380.1) Source type: large scale study Cross-references: | |||||||
ENSVATH10585240 | 542 | A>T | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.08) Somatic: No Accession: 3:g.3224540C>T Codon: GCT/ACT Consequence type: missense Cytogenetic band: Genomic location: 3:g.3224540C>T Locations: - p.Ala542Thr (EnsemblPlants:AT3G10380.1) - c.1624G>A (EnsemblPlants:AT3G10380.1) Source type: large scale study Cross-references: | |||||||
ENSVATH00315118 | 556 | A>T | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.06) Somatic: No Accession: 3:g.3224002C>T Codon: GCA/ACA Consequence type: missense Cytogenetic band: Genomic location: 3:g.3224002C>T Locations: - p.Ala556Thr (EnsemblPlants:AT3G10380.1) - c.1666G>A (EnsemblPlants:AT3G10380.1) Source type: large scale study Cross-references: | |||||||
ENSVATH00315115 | 635 | S>C | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.02) Somatic: No Accession: 3:g.3223605G>C Codon: TCC/TGC Consequence type: missense Cytogenetic band: Genomic location: 3:g.3223605G>C Locations: - p.Ser635Cys (EnsemblPlants:AT3G10380.1) - c.1904C>G (EnsemblPlants:AT3G10380.1) Source type: large scale study Cross-references: | |||||||
tmp_3_3223603_G_A | 636 | Q>* | 1000Genomes | ||||
Consequence: stop gained Somatic: No Accession: 3:g.3223603G>A Codon: CAG/TAG Consequence type: stop gained Cytogenetic band: Genomic location: 3:g.3223603G>A Locations: - p.Gln636Ter (EnsemblPlants:AT3G10380.1) - c.1906C>T (EnsemblPlants:AT3G10380.1) Source type: large scale study Cross-references: | |||||||
ENSVATH05803579 | 636 | Q>L | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.12) Somatic: No Accession: 3:g.3223602T>A Codon: CAG/CTG Consequence type: missense Cytogenetic band: Genomic location: 3:g.3223602T>A Locations: - p.Gln636Leu (EnsemblPlants:AT3G10380.1) - c.1907A>T (EnsemblPlants:AT3G10380.1) Source type: large scale study Cross-references: | |||||||
tmp_3_3223352_T_G | 670 | I>L | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.25) Somatic: No Accession: 3:g.3223352T>G Codon: ATA/CTA Consequence type: missense Cytogenetic band: Genomic location: 3:g.3223352T>G Locations: - p.Ile670Leu (EnsemblPlants:AT3G10380.1) - c.2008A>C (EnsemblPlants:AT3G10380.1) Source type: large scale study Cross-references: | |||||||
tmp_3_3222929_C_T,G | 680 | A>P | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.29) Somatic: No Accession: 3:g.3222929C>G Codon: GCA/CCA Consequence type: missense Cytogenetic band: Genomic location: 3:g.3222929C>G Locations: - p.Ala680Pro (EnsemblPlants:AT3G10380.1) - c.2038G>C (EnsemblPlants:AT3G10380.1) Source type: large scale study Cross-references: | |||||||
tmp_3_3222929_C_T,G | 680 | A>T | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.13) Somatic: No Accession: 3:g.3222929C>T Codon: GCA/ACA Consequence type: missense Cytogenetic band: Genomic location: 3:g.3222929C>T Locations: - p.Ala680Thr (EnsemblPlants:AT3G10380.1) - c.2038G>A (EnsemblPlants:AT3G10380.1) Source type: large scale study Cross-references: | |||||||
ENSVATH10585206 | 681 | H>Y | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.18) Somatic: No Accession: 3:g.3222926G>A Codon: CAT/TAT Consequence type: missense Cytogenetic band: Genomic location: 3:g.3222926G>A Locations: - p.His681Tyr (EnsemblPlants:AT3G10380.1) - c.2041C>T (EnsemblPlants:AT3G10380.1) Source type: large scale study Cross-references: | |||||||
tmp_3_3222621_T_A | 722 | D>V | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.01) Somatic: No Accession: 3:g.3222621T>A Codon: GAT/GTT Consequence type: missense Cytogenetic band: Genomic location: 3:g.3222621T>A Locations: - p.Asp722Val (EnsemblPlants:AT3G10380.1) - c.2165A>T (EnsemblPlants:AT3G10380.1) Source type: large scale study Cross-references: | |||||||
tmp_3_3222050_C_A | 763 | L>F | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.04) Somatic: No Accession: 3:g.3222050C>A Codon: TTG/TTT Consequence type: missense Cytogenetic band: Genomic location: 3:g.3222050C>A Locations: - p.Leu763Phe (EnsemblPlants:AT3G10380.1) - c.2289G>T (EnsemblPlants:AT3G10380.1) Source type: large scale study Cross-references: | |||||||
ENSVATH10585177 | 763 | L>M | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.13) Somatic: No Accession: 3:g.3222052A>T Codon: TTG/ATG Consequence type: missense Cytogenetic band: Genomic location: 3:g.3222052A>T Locations: - p.Leu763Met (EnsemblPlants:AT3G10380.1) - c.2287T>A (EnsemblPlants:AT3G10380.1) Source type: large scale study Cross-references: | |||||||
ENSVATH05803566 | 776 | T>A | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.42) Somatic: No Accession: 3:g.3222013T>C Codon: ACG/GCG Consequence type: missense Cytogenetic band: Genomic location: 3:g.3222013T>C Locations: - p.Thr776Ala (EnsemblPlants:AT3G10380.1) - c.2326A>G (EnsemblPlants:AT3G10380.1) Source type: large scale study Cross-references: | |||||||
tmp_3_3221983_C_A | 786 | A>S | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.65) Somatic: No Accession: 3:g.3221983C>A Codon: GCT/TCT Consequence type: missense Cytogenetic band: Genomic location: 3:g.3221983C>A Locations: - p.Ala786Ser (EnsemblPlants:AT3G10380.1) - c.2356G>T (EnsemblPlants:AT3G10380.1) Source type: large scale study Cross-references: | |||||||
ENSVATH00315109 | 797 | F>L | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (1) Somatic: No Accession: 3:g.3221950A>G Codon: TTC/CTC Consequence type: missense Cytogenetic band: Genomic location: 3:g.3221950A>G Locations: - p.Phe797Leu (EnsemblPlants:AT3G10380.1) - c.2389T>C (EnsemblPlants:AT3G10380.1) Source type: large scale study Cross-references: | |||||||
tmp_3_3221943_C_T | 799 | S>N | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (1) Somatic: No Accession: 3:g.3221943C>T Codon: AGT/AAT Consequence type: missense Cytogenetic band: Genomic location: 3:g.3221943C>T Locations: - p.Ser799Asn (EnsemblPlants:AT3G10380.1) - c.2396G>A (EnsemblPlants:AT3G10380.1) Source type: large scale study Cross-references: | |||||||
tmp_3_3221822_T_C | 813 | N>S | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.14) Somatic: No Accession: 3:g.3221822T>C Codon: AAC/AGC Consequence type: missense Cytogenetic band: Genomic location: 3:g.3221822T>C Locations: - p.Asn813Ser (EnsemblPlants:AT3G10380.1) - c.2438A>G (EnsemblPlants:AT3G10380.1) Source type: large scale study Cross-references: | |||||||
ENSVATH13892737 | 832 | I>S | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 3:g.3221765A>C Codon: ATT/AGT Consequence type: missense Cytogenetic band: Genomic location: 3:g.3221765A>C Locations: - p.Ile832Ser (EnsemblPlants:AT3G10380.1) - c.2495T>G (EnsemblPlants:AT3G10380.1) Source type: large scale study Cross-references: | |||||||
tmp_3_3221356_C_T | 841 | R>H | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.12) Somatic: No Accession: 3:g.3221356C>T Codon: CGT/CAT Consequence type: missense Cytogenetic band: Genomic location: 3:g.3221356C>T Locations: - p.Arg841His (EnsemblPlants:AT3G10380.1) - c.2522G>A (EnsemblPlants:AT3G10380.1) Source type: large scale study Cross-references: | |||||||
ENSVATH05803561 | 843 | A>V | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.29) Somatic: No Accession: 3:g.3221350G>A Codon: GCG/GTG Consequence type: missense Cytogenetic band: Genomic location: 3:g.3221350G>A Locations: - p.Ala843Val (EnsemblPlants:AT3G10380.1) - c.2528C>T (EnsemblPlants:AT3G10380.1) Source type: large scale study Cross-references: | |||||||
tmp_3_3221335_C_G | 848 | G>A | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.67) Somatic: No Accession: 3:g.3221335C>G Codon: GGT/GCT Consequence type: missense Cytogenetic band: Genomic location: 3:g.3221335C>G Locations: - p.Gly848Ala (EnsemblPlants:AT3G10380.1) - c.2543G>C (EnsemblPlants:AT3G10380.1) Source type: large scale study Cross-references: | |||||||
ENSVATH10585170 | 851 | R>G | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.03) Somatic: No Accession: 3:g.3221327T>C Codon: AGA/GGA Consequence type: missense Cytogenetic band: Genomic location: 3:g.3221327T>C Locations: - p.Arg851Gly (EnsemblPlants:AT3G10380.1) - c.2551A>G (EnsemblPlants:AT3G10380.1) Source type: large scale study Cross-references: | |||||||
tmp_3_3221317_G_T | 854 | A>E | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.26) Somatic: No Accession: 3:g.3221317G>T Codon: GCA/GAA Consequence type: missense Cytogenetic band: Genomic location: 3:g.3221317G>T Locations: - p.Ala854Glu (EnsemblPlants:AT3G10380.1) - c.2561C>A (EnsemblPlants:AT3G10380.1) Source type: large scale study Cross-references: | |||||||
tmp_3_3221303_T_A | 859 | N>Y | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.07) Somatic: No Accession: 3:g.3221303T>A Codon: AAT/TAT Consequence type: missense Cytogenetic band: Genomic location: 3:g.3221303T>A Locations: - p.Asn859Tyr (EnsemblPlants:AT3G10380.1) - c.2575A>T (EnsemblPlants:AT3G10380.1) Source type: large scale study Cross-references: | |||||||
tmp_3_3221287_G_T | 864 | A>E | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.01) Somatic: No Accession: 3:g.3221287G>T Codon: GCA/GAA Consequence type: missense Cytogenetic band: Genomic location: 3:g.3221287G>T Locations: - p.Ala864Glu (EnsemblPlants:AT3G10380.1) - c.2591C>A (EnsemblPlants:AT3G10380.1) Source type: large scale study Cross-references: | |||||||
tmp_3_3221076_C_G | 902 | E>Q | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (1) Somatic: No Accession: 3:g.3221076C>G Codon: GAG/CAG Consequence type: missense Cytogenetic band: Genomic location: 3:g.3221076C>G Locations: - p.Glu902Gln (EnsemblPlants:AT3G10380.1) - c.2704G>C (EnsemblPlants:AT3G10380.1) Source type: large scale study Cross-references: | |||||||
tmp_3_3220714_T_A | 929 | I>F | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.01) Somatic: No Accession: 3:g.3220714T>A Codon: ATC/TTC Consequence type: missense Cytogenetic band: Genomic location: 3:g.3220714T>A Locations: - p.Ile929Phe (EnsemblPlants:AT3G10380.1) - c.2785A>T (EnsemblPlants:AT3G10380.1) Source type: large scale study Cross-references: | |||||||
tmp_3_3220656_G_A | 948 | A>V | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.19) Somatic: No Accession: 3:g.3220656G>A Codon: GCG/GTG Consequence type: missense Cytogenetic band: Genomic location: 3:g.3220656G>A Locations: - p.Ala948Val (EnsemblPlants:AT3G10380.1) - c.2843C>T (EnsemblPlants:AT3G10380.1) Source type: large scale study Cross-references: | |||||||
ENSVATH13892703 | 973 | A>T | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 3:g.3220455C>T Codon: GCA/ACA Consequence type: missense Cytogenetic band: Genomic location: 3:g.3220455C>T Locations: - p.Ala973Thr (EnsemblPlants:AT3G10380.1) - c.2917G>A (EnsemblPlants:AT3G10380.1) Source type: large scale study Cross-references: | |||||||
ENSVATH10585140 | 997 | R>H | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 3:g.3220307C>T Codon: CGT/CAT Consequence type: missense Cytogenetic band: Genomic location: 3:g.3220307C>T Locations: - p.Arg997His (EnsemblPlants:AT3G10380.1) - c.2990G>A (EnsemblPlants:AT3G10380.1) Source type: large scale study Cross-references: | |||||||
ENSVATH13892701 | 1012 | A>V | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.08) Somatic: No Accession: 3:g.3220159G>A Codon: GCT/GTT Consequence type: missense Cytogenetic band: Genomic location: 3:g.3220159G>A Locations: - p.Ala1012Val (EnsemblPlants:AT3G10380.1) - c.3035C>T (EnsemblPlants:AT3G10380.1) Source type: large scale study Cross-references: | |||||||
tmp_3_3220143_G_T | 1017 | H>Q | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.07) Somatic: No Accession: 3:g.3220143G>T Codon: CAC/CAA Consequence type: missense Cytogenetic band: Genomic location: 3:g.3220143G>T Locations: - p.His1017Gln (EnsemblPlants:AT3G10380.1) - c.3051C>A (EnsemblPlants:AT3G10380.1) Source type: large scale study Cross-references: | |||||||
tmp_3_3220142_C_A | 1018 | D>Y | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 3:g.3220142C>A Codon: GAC/TAC Consequence type: missense Cytogenetic band: Genomic location: 3:g.3220142C>A Locations: - p.Asp1018Tyr (EnsemblPlants:AT3G10380.1) - c.3052G>T (EnsemblPlants:AT3G10380.1) Source type: large scale study Cross-references: | |||||||
ENSVATH10585137 | 1020 | M>I | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.3) Somatic: No Accession: 3:g.3220134C>T Codon: ATG/ATA Consequence type: missense Cytogenetic band: Genomic location: 3:g.3220134C>T Locations: - p.Met1020Ile (EnsemblPlants:AT3G10380.1) - c.3060G>A (EnsemblPlants:AT3G10380.1) Source type: large scale study Cross-references: | |||||||
ENSVATH10585136 | 1034 | V>I | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.06) Somatic: No Accession: 3:g.3219984C>T Codon: GTT/ATT Consequence type: missense Cytogenetic band: Genomic location: 3:g.3219984C>T Locations: - p.Val1034Ile (EnsemblPlants:AT3G10380.1) - c.3100G>A (EnsemblPlants:AT3G10380.1) Source type: large scale study Cross-references: |