W5P9G9 · W5P9G9_SHEEP
- ProteinInsulin-induced gene protein
- GeneINSIG1
- StatusUniProtKB unreviewed (TrEMBL)
- Organism
- Amino acids276 (go to sequence)
- Protein existenceInferred from homology
- Annotation score3/5
Variants
Variant ID(s) | Position(s) | Change | Description | Clinical significance | Provenance | ||
---|---|---|---|---|---|---|---|
rs159818455 | 27 | T>A | Ensembl | ||||
Consequence: missense Predictions: - SIFT: tolerated - low confidence (1) Somatic: No Accession: NC_019461.1:g.116528764A>G Codon: ACC/GCC Consequence type: missense Cytogenetic band: Genomic location: NC_019461.1:g.116528764A>G Locations: - p.Thr27Ala (Ensembl:ENSOART00000007184) - c.79A>G (Ensembl:ENSOART00000007184) Source type: large scale study Cross-references: | |||||||
rs1089206462 | 98 | A>V | Ensembl | ||||
Consequence: missense Predictions: - SIFT: deleterious - low confidence (0.03) Somatic: No Accession: NC_019461.1:g.116528978C>T Codon: GCC/GTC Consequence type: missense Cytogenetic band: Genomic location: NC_019461.1:g.116528978C>T Locations: - p.Ala98Val (Ensembl:ENSOART00000007184) - c.293C>T (Ensembl:ENSOART00000007184) Source type: large scale study Cross-references: | |||||||
rs1092020149 | 193 | A>V | Ensembl | ||||
Consequence: missense Predictions: - SIFT: deleterious - low confidence (0.03) Somatic: No Accession: NC_019461.1:g.116533063C>T Codon: GCA/GTA Consequence type: missense Cytogenetic band: Genomic location: NC_019461.1:g.116533063C>T Locations: - p.Ala193Val (Ensembl:ENSOART00000007184) - c.578C>T (Ensembl:ENSOART00000007184) Source type: large scale study Cross-references: | |||||||
rs1089600034 | 200 | W>* | Ensembl | ||||
Consequence: stop gained Somatic: No Accession: NC_019461.1:g.116533085G>A Codon: TGG/TGA Consequence type: stop gained Cytogenetic band: Genomic location: NC_019461.1:g.116533085G>A Locations: - p.Trp200Ter (Ensembl:ENSOART00000007184) - c.600G>A (Ensembl:ENSOART00000007184) Source type: large scale study Cross-references: | |||||||
rs599329416 | 233 | Y>C | Ensembl | ||||
Consequence: missense Predictions: - SIFT: deleterious - low confidence (0.02) Somatic: No Accession: NC_019461.1:g.116533183A>G Codon: TAT/TGT Consequence type: missense Cytogenetic band: Genomic location: NC_019461.1:g.116533183A>G Locations: - p.Tyr233Cys (Ensembl:ENSOART00000007184) - c.698A>G (Ensembl:ENSOART00000007184) Source type: large scale study Cross-references: | |||||||
rs591430379 | 236 | T>S | Ensembl | ||||
Consequence: missense Predictions: - SIFT: deleterious - low confidence (0.04) Somatic: No Accession: NC_019461.1:g.116533720A>T Codon: ACG/TCG Consequence type: missense Cytogenetic band: Genomic location: NC_019461.1:g.116533720A>T Locations: - p.Thr236Ser (Ensembl:ENSOART00000007184) - c.706A>T (Ensembl:ENSOART00000007184) Source type: large scale study Cross-references: |