A0A338P733 · A0A338P733_MOUSE
- ProteinKininogen 2
- GeneKng2
- StatusUniProtKB unreviewed (TrEMBL)
- Organism
- Amino acids
- Protein existenceEvidence at protein level
- Annotation score1/5
Variants
Variant ID(s) | Position(s) | Change | Description | Clinical significance | Provenance | ||
---|---|---|---|---|---|---|---|
rs49512699 | 5 | A>P | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated - low confidence (0.17) Somatic: No Accession: NC_000082.7:g.22845899C>G Codon: GCA/CCA Consequence type: missense Cytogenetic band: 16q Genomic location: NC_000082.7:g.22845899C>G Locations: - p.Ala5Pro (Ensembl:ENSMUST00000231835) - c.13G>C (Ensembl:ENSMUST00000231835) Source type: large scale study Cross-references: | |||||||
rs52056094 | 25 | L>V | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated - low confidence (0.24) Somatic: No Accession: NC_000082.7:g.22845839G>C Codon: CTG/GTG Consequence type: missense Cytogenetic band: 16q Genomic location: NC_000082.7:g.22845839G>C Locations: - p.Leu25Val (Ensembl:ENSMUST00000231835) - c.73C>G (Ensembl:ENSMUST00000231835) Source type: large scale study Cross-references: | |||||||
rs46533264 | 35 | S>A | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated - low confidence (1) Somatic: No Accession: NC_000082.7:g.22845809A>C Codon: TCT/GCT Consequence type: missense Cytogenetic band: 16q Genomic location: NC_000082.7:g.22845809A>C Locations: - p.Ser35Ala (Ensembl:ENSMUST00000231835) - c.103T>G (Ensembl:ENSMUST00000231835) Source type: large scale study Cross-references: |