A0A5G2R179 · A0A5G2R179_PIG
- ProteinLipoprotein lipase
- GeneLPL
- StatusUniProtKB unreviewed (TrEMBL)
- Organism
- Amino acids452 (go to sequence)
- Protein existenceInferred from homology
- Annotation score4/5
Variants
Variant ID(s) | Position(s) | Change | Description | Clinical significance | Provenance | ||
---|---|---|---|---|---|---|---|
rs3475593045 | 27 | T>P | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.13) Somatic: No Accession: NC_010456.5:g.4105038A>C Codon: ACC/CCC Consequence type: missense Cytogenetic band: Genomic location: NC_010456.5:g.4105038A>C Locations: - p.Thr27Pro (Ensembl:ENSSSCT00000071711) - c.79A>C (Ensembl:ENSSSCT00000071711) Source type: large scale study Cross-references: | |||||||
rs3472872251 | 148 | E>V | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.12) Somatic: No Accession: NC_010456.5:g.4122389A>T Codon: GAA/GTA Consequence type: missense Cytogenetic band: Genomic location: NC_010456.5:g.4122389A>T Locations: - p.Glu148Val (Ensembl:ENSSSCT00000071711) - c.443A>T (Ensembl:ENSSSCT00000071711) Source type: large scale study Cross-references: | |||||||
rs3474195007 | 150 | N>S | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.09) Somatic: No Accession: NC_010456.5:g.4122395A>G Codon: AAC/AGC Consequence type: missense Cytogenetic band: Genomic location: NC_010456.5:g.4122395A>G Locations: - p.Asn150Ser (Ensembl:ENSSSCT00000071711) - c.449A>G (Ensembl:ENSSSCT00000071711) Source type: large scale study Cross-references: | |||||||
rs3474464009 | 448 | I>V | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated - low confidence (0.54) Somatic: No Accession: NC_010456.5:g.4129383A>G Codon: ATT/GTT Consequence type: missense Cytogenetic band: Genomic location: NC_010456.5:g.4129383A>G Locations: - p.Ile448Val (Ensembl:ENSSSCT00000071711) - c.1342A>G (Ensembl:ENSSSCT00000071711) Source type: large scale study Cross-references: | |||||||
rs3476431208 | 452 | R>L | EVA | ||||
Consequence: missense Somatic: No Accession: NC_010456.5:g.4129396G>T Codon: CGT/CTT Consequence type: missense Cytogenetic band: Genomic location: NC_010456.5:g.4129396G>T Locations: - p.Arg452Leu (Ensembl:ENSSSCT00000071711) - c.1355G>T (Ensembl:ENSSSCT00000071711) Source type: large scale study Cross-references: |