Q9LK50 · AB26G_ARATH
- ProteinABC transporter G family member 26
- GeneABCG26
- StatusUniProtKB reviewed (Swiss-Prot)
- Amino acids685 (go to sequence)
- Protein existenceEvidence at transcript level
- Annotation score5/5
Variants
Variant ID(s) | Position(s) | Change | Description | Clinical significance | Provenance | ||
---|---|---|---|---|---|---|---|
tmp_3_4250667_T_C | 13 | N>D | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated - low confidence (0.12) Somatic: No Accession: 3:g.4250667T>C Codon: AAT/GAT Consequence type: missense Cytogenetic band: Genomic location: 3:g.4250667T>C Locations: - p.Asn13Asp (EnsemblPlants:AT3G13220.1) - c.37A>G (EnsemblPlants:AT3G13220.1) Source type: large scale study Cross-references: | |||||||
ENSVATH00320554 | 23 | G>D | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.18) Somatic: No Accession: 3:g.4250636C>T Codon: GGC/GAC Consequence type: missense Cytogenetic band: Genomic location: 3:g.4250636C>T Locations: - p.Gly23Asp (EnsemblPlants:AT3G13220.1) - c.68G>A (EnsemblPlants:AT3G13220.1) Source type: large scale study Cross-references: | |||||||
ENSVATH13908375 | 53 | T>S | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.94) Somatic: No Accession: 3:g.4250546G>C Codon: ACT/AGT Consequence type: missense Cytogenetic band: Genomic location: 3:g.4250546G>C Locations: - p.Thr53Ser (EnsemblPlants:AT3G13220.1) - c.158C>G (EnsemblPlants:AT3G13220.1) Source type: large scale study Cross-references: | |||||||
ENSVATH05820373 | 57 | E>K | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.91) Somatic: No Accession: 3:g.4250535C>T Codon: GAA/AAA Consequence type: missense Cytogenetic band: Genomic location: 3:g.4250535C>T Locations: - p.Glu57Lys (EnsemblPlants:AT3G13220.1) - c.169G>A (EnsemblPlants:AT3G13220.1) Source type: large scale study Cross-references: | |||||||
ENSVATH10645984 | 60 | P>S | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.27) Somatic: No Accession: 3:g.4250526G>A Codon: CCT/TCT Consequence type: missense Cytogenetic band: Genomic location: 3:g.4250526G>A Locations: - p.Pro60Ser (EnsemblPlants:AT3G13220.1) - c.178C>T (EnsemblPlants:AT3G13220.1) Source type: large scale study Cross-references: | |||||||
tmp_3_4250515_G_C | 63 | I>M | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 3:g.4250515G>C Codon: ATC/ATG Consequence type: missense Cytogenetic band: Genomic location: 3:g.4250515G>C Locations: - p.Ile63Met (EnsemblPlants:AT3G13220.1) - c.189C>G (EnsemblPlants:AT3G13220.1) Source type: large scale study Cross-references: | |||||||
ENSVATH05820372 | 73 | K>Q | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.02) Somatic: No Accession: 3:g.4250408T>G Codon: AAG/CAG Consequence type: missense Cytogenetic band: Genomic location: 3:g.4250408T>G Locations: - p.Lys73Gln (EnsemblPlants:AT3G13220.1) - c.217A>C (EnsemblPlants:AT3G13220.1) Source type: large scale study Cross-references: | |||||||
tmp_3_4250323_T_A | 101 | D>V | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.05) Somatic: No Accession: 3:g.4250323T>A Codon: GAT/GTT Consequence type: missense Cytogenetic band: Genomic location: 3:g.4250323T>A Locations: - p.Asp101Val (EnsemblPlants:AT3G13220.1) - c.302A>T (EnsemblPlants:AT3G13220.1) Source type: large scale study Cross-references: | |||||||
tmp_3_4250317_T_C | 103 | Y>C | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.21) Somatic: No Accession: 3:g.4250317T>C Codon: TAC/TGC Consequence type: missense Cytogenetic band: Genomic location: 3:g.4250317T>C Locations: - p.Tyr103Cys (EnsemblPlants:AT3G13220.1) - c.308A>G (EnsemblPlants:AT3G13220.1) Source type: large scale study Cross-references: | |||||||
ENSVATH13908353 | 162 | R>S | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.17) Somatic: No Accession: 3:g.4250139C>A Codon: AGG/AGT Consequence type: missense Cytogenetic band: Genomic location: 3:g.4250139C>A Locations: - p.Arg162Ser (EnsemblPlants:AT3G13220.1) - c.486G>T (EnsemblPlants:AT3G13220.1) Source type: large scale study Cross-references: | |||||||
tmp_3_4249955_G_A | 202 | A>V | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.06) Somatic: No Accession: 3:g.4249955G>A Codon: GCC/GTC Consequence type: missense Cytogenetic band: Genomic location: 3:g.4249955G>A Locations: - p.Ala202Val (EnsemblPlants:AT3G13220.1) - c.605C>T (EnsemblPlants:AT3G13220.1) Source type: large scale study Cross-references: | |||||||
tmp_3_4249779_G_A | 217 | R>C | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.02) Somatic: No Accession: 3:g.4249779G>A Codon: CGT/TGT Consequence type: missense Cytogenetic band: Genomic location: 3:g.4249779G>A Locations: - p.Arg217Cys (EnsemblPlants:AT3G13220.1) - c.649C>T (EnsemblPlants:AT3G13220.1) Source type: large scale study Cross-references: | |||||||
ENSVATH07960082 | 225 | F>I | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.02) Somatic: No Accession: 3:g.4249755A>T Codon: TTT/ATT Consequence type: missense Cytogenetic band: Genomic location: 3:g.4249755A>T Locations: - p.Phe225Ile (EnsemblPlants:AT3G13220.1) - c.673T>A (EnsemblPlants:AT3G13220.1) Source type: large scale study Cross-references: | |||||||
tmp_3_4249749_T_G | 227 | K>Q | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.01) Somatic: No Accession: 3:g.4249749T>G Codon: AAG/CAG Consequence type: missense Cytogenetic band: Genomic location: 3:g.4249749T>G Locations: - p.Lys227Gln (EnsemblPlants:AT3G13220.1) - c.679A>C (EnsemblPlants:AT3G13220.1) Source type: large scale study Cross-references: | |||||||
tmp_3_4249489_T_C | 285 | I>V | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 3:g.4249489T>C Codon: ATT/GTT Consequence type: missense Cytogenetic band: Genomic location: 3:g.4249489T>C Locations: - p.Ile285Val (EnsemblPlants:AT3G13220.1) - c.853A>G (EnsemblPlants:AT3G13220.1) Source type: large scale study Cross-references: | |||||||
ENSVATH00320550 | 307 | P>L | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.37) Somatic: No Accession: 3:g.4249422G>A Codon: CCT/CTT Consequence type: missense Cytogenetic band: Genomic location: 3:g.4249422G>A Locations: - p.Pro307Leu (EnsemblPlants:AT3G13220.1) - c.920C>T (EnsemblPlants:AT3G13220.1) Source type: large scale study Cross-references: | |||||||
ENSVATH05820366 | 341 | A>T | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 3:g.4249321C>T Codon: GCA/ACA Consequence type: missense Cytogenetic band: Genomic location: 3:g.4249321C>T Locations: - p.Ala341Thr (EnsemblPlants:AT3G13220.1) - c.1021G>A (EnsemblPlants:AT3G13220.1) Source type: large scale study Cross-references: | |||||||
ENSVATH05820365 | 344 | Q>K | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.78) Somatic: No Accession: 3:g.4249312G>T Codon: CAA/AAA Consequence type: missense Cytogenetic band: Genomic location: 3:g.4249312G>T Locations: - p.Gln344Lys (EnsemblPlants:AT3G13220.1) - c.1030C>A (EnsemblPlants:AT3G13220.1) Source type: large scale study Cross-references: | |||||||
ENSVATH00320549 | 355 | L>F | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.77) Somatic: No Accession: 3:g.4249277C>A Codon: TTG/TTT Consequence type: missense Cytogenetic band: Genomic location: 3:g.4249277C>A Locations: - p.Leu355Phe (EnsemblPlants:AT3G13220.1) - c.1065G>T (EnsemblPlants:AT3G13220.1) Source type: large scale study Cross-references: | |||||||
ENSVATH05820364 | 375 | R>S | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.52) Somatic: No Accession: 3:g.4249146C>G Codon: AGG/AGC Consequence type: missense Cytogenetic band: Genomic location: 3:g.4249146C>G Locations: - p.Arg375Ser (EnsemblPlants:AT3G13220.1) - c.1125G>C (EnsemblPlants:AT3G13220.1) Source type: large scale study Cross-references: | |||||||
tmp_3_4249133_A_T | 380 | L>M | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 3:g.4249133A>T Codon: TTG/ATG Consequence type: missense Cytogenetic band: Genomic location: 3:g.4249133A>T Locations: - p.Leu380Met (EnsemblPlants:AT3G13220.1) - c.1138T>A (EnsemblPlants:AT3G13220.1) Source type: large scale study Cross-references: | |||||||
tmp_3_4249129_T_G | 381 | E>A | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.96) Somatic: No Accession: 3:g.4249129T>G Codon: GAG/GCG Consequence type: missense Cytogenetic band: Genomic location: 3:g.4249129T>G Locations: - p.Glu381Ala (EnsemblPlants:AT3G13220.1) - c.1142A>C (EnsemblPlants:AT3G13220.1) Source type: large scale study Cross-references: | |||||||
tmp_3_4249067_T_A | 402 | I>F | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.15) Somatic: No Accession: 3:g.4249067T>A Codon: ATC/TTC Consequence type: missense Cytogenetic band: Genomic location: 3:g.4249067T>A Locations: - p.Ile402Phe (EnsemblPlants:AT3G13220.1) - c.1204A>T (EnsemblPlants:AT3G13220.1) Source type: large scale study Cross-references: | |||||||
ENSVATH02138877 | 414 | D>N | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.04) Somatic: No Accession: 3:g.4249031C>T Codon: GAT/AAT Consequence type: missense Cytogenetic band: Genomic location: 3:g.4249031C>T Locations: - p.Asp414Asn (EnsemblPlants:AT3G13220.1) - c.1240G>A (EnsemblPlants:AT3G13220.1) Source type: large scale study Cross-references: | |||||||
tmp_3_4248904_G_A | 456 | T>I | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.39) Somatic: No Accession: 3:g.4248904G>A Codon: ACA/ATA Consequence type: missense Cytogenetic band: Genomic location: 3:g.4248904G>A Locations: - p.Thr456Ile (EnsemblPlants:AT3G13220.1) - c.1367C>T (EnsemblPlants:AT3G13220.1) Source type: large scale study Cross-references: | |||||||
tmp_3_4248760_C_A | 476 | W>C | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 3:g.4248760C>A Codon: TGG/TGT Consequence type: missense Cytogenetic band: Genomic location: 3:g.4248760C>A Locations: - p.Trp476Cys (EnsemblPlants:AT3G13220.1) - c.1428G>T (EnsemblPlants:AT3G13220.1) Source type: large scale study Cross-references: | |||||||
tmp_3_4248717_C_T | 491 | E>K | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: 3:g.4248717C>T Codon: GAG/AAG Consequence type: missense Cytogenetic band: Genomic location: 3:g.4248717C>T Locations: - p.Glu491Lys (EnsemblPlants:AT3G13220.1) - c.1471G>A (EnsemblPlants:AT3G13220.1) Source type: large scale study Cross-references: | |||||||
tmp_3_4248634_C_T | 518 | M>I | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.04) Somatic: No Accession: 3:g.4248634C>T Codon: ATG/ATA Consequence type: missense Cytogenetic band: Genomic location: 3:g.4248634C>T Locations: - p.Met518Ile (EnsemblPlants:AT3G13220.1) - c.1554G>A (EnsemblPlants:AT3G13220.1) Source type: large scale study Cross-references: | |||||||
tmp_3_4248611_G_A | 526 | T>I | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.26) Somatic: No Accession: 3:g.4248611G>A Codon: ACA/ATA Consequence type: missense Cytogenetic band: Genomic location: 3:g.4248611G>A Locations: - p.Thr526Ile (EnsemblPlants:AT3G13220.1) - c.1577C>T (EnsemblPlants:AT3G13220.1) Source type: large scale study Cross-references: | |||||||
tmp_3_4248562_G_C | 542 | I>M | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.17) Somatic: No Accession: 3:g.4248562G>C Codon: ATC/ATG Consequence type: missense Cytogenetic band: Genomic location: 3:g.4248562G>C Locations: - p.Ile542Met (EnsemblPlants:AT3G13220.1) - c.1626C>G (EnsemblPlants:AT3G13220.1) Source type: large scale study Cross-references: | |||||||
ENSVATH00320547 | 649 | I>V | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated (1) Somatic: No Accession: 3:g.4248081T>C Codon: ATA/GTA Consequence type: missense Cytogenetic band: Genomic location: 3:g.4248081T>C Locations: - p.Ile649Val (EnsemblPlants:AT3G13220.1) - c.1945A>G (EnsemblPlants:AT3G13220.1) Source type: large scale study Cross-references: | |||||||
ENSVATH13908347 | 673 | Y>F | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.01) Somatic: No Accession: 3:g.4248008T>A Codon: TAC/TTC Consequence type: missense Cytogenetic band: Genomic location: 3:g.4248008T>A Locations: - p.Tyr673Phe (EnsemblPlants:AT3G13220.1) - c.2018A>T (EnsemblPlants:AT3G13220.1) Source type: large scale study Cross-references: | |||||||
tmp_3_4247982_T_A | 682 | I>F | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated - low confidence (0.17) Somatic: No Accession: 3:g.4247982T>A Codon: ATT/TTT Consequence type: missense Cytogenetic band: Genomic location: 3:g.4247982T>A Locations: - p.Ile682Phe (EnsemblPlants:AT3G13220.1) - c.2044A>T (EnsemblPlants:AT3G13220.1) Source type: large scale study Cross-references: | |||||||
tmp_3_4247976_G_C | 684 | H>D | 1000Genomes | ||||
Consequence: missense Predictions: - SIFT: tolerated - low confidence (0.65) Somatic: No Accession: 3:g.4247976G>C Codon: CAT/GAT Consequence type: missense Cytogenetic band: Genomic location: 3:g.4247976G>C Locations: - p.His684Asp (EnsemblPlants:AT3G13220.1) - c.2050C>G (EnsemblPlants:AT3G13220.1) Source type: large scale study Cross-references: |