P42838 · LEM3_YEAST
- ProteinPhospholipid-transporting ATPase accessory subunit LEM3
- GeneLEM3
- StatusUniProtKB reviewed (Swiss-Prot)
- Amino acids414 (go to sequence)
- Protein existenceEvidence at protein level
- Annotation score5/5
Variants
Variant ID(s) | Position(s) | Change | Description | Clinical significance | Provenance | ||
---|---|---|---|---|---|---|---|
s14-32007 | 22 | V>E | SGRP | ||||
Consequence: missense Predictions: - SIFT: tolerated (1) Somatic: No Accession: XIV:g.32008T>A Codon: GTG/GAG Consequence type: missense Cytogenetic band: Genomic location: XIV:g.32008T>A Locations: - p.Val22Glu (Ensembl:YNL323W_mRNA) - c.65T>A (Ensembl:YNL323W_mRNA) Source type: large scale study Cross-references: - SGRP: s14-32007 | |||||||
s14-32111 | 57 | A>T | SGRP | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.48) Somatic: No Accession: XIV:g.32112G>A Codon: GCA/ACA Consequence type: missense Cytogenetic band: Genomic location: XIV:g.32112G>A Locations: - p.Ala57Thr (Ensembl:YNL323W_mRNA) - c.169G>A (Ensembl:YNL323W_mRNA) Source type: large scale study Cross-references: - SGRP: s14-32111 | |||||||
s14-32264 | 108 | Q>E | SGRP | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.81) Somatic: No Accession: XIV:g.32265C>G Codon: CAG/GAG Consequence type: missense Cytogenetic band: Genomic location: XIV:g.32265C>G Locations: - p.Gln108Glu (Ensembl:YNL323W_mRNA) - c.322C>G (Ensembl:YNL323W_mRNA) Source type: large scale study Cross-references: - SGRP: s14-32264 | |||||||
s14-32409 | 156 | R>K | SGRP | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.73) Somatic: No Accession: XIV:g.32410G>A Codon: AGA/AAA Consequence type: missense Cytogenetic band: Genomic location: XIV:g.32410G>A Locations: - p.Arg156Lys (Ensembl:YNL323W_mRNA) - c.467G>A (Ensembl:YNL323W_mRNA) Source type: large scale study Cross-references: - SGRP: s14-32409 | |||||||
s14-32976 | 345 | G>D | SGRP | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.39) Somatic: No Accession: XIV:g.32977G>A Codon: GGT/GAT Consequence type: missense Cytogenetic band: Genomic location: XIV:g.32977G>A Locations: - p.Gly345Asp (Ensembl:YNL323W_mRNA) - c.1034G>A (Ensembl:YNL323W_mRNA) Source type: large scale study Cross-references: - SGRP: s14-32976 |