P53122 · YGN8_YEAST
- ProteinUncharacterized protein YGL138C
- StatusUniProtKB reviewed (Swiss-Prot)
- Amino acids345 (go to sequence)
- Protein existencePredicted
- Annotation score1/5
Variants
Variant ID(s) | Position(s) | Change | Description | Clinical significance | Provenance | ||
---|---|---|---|---|---|---|---|
s07-249455 | 28 | F>L | SGRP | ||||
Consequence: missense Predictions: - SIFT: tolerated - low confidence (1) Somatic: No Accession: VII:g.249450A>G Codon: TTT/CTT Consequence type: missense Cytogenetic band: Genomic location: VII:g.249450A>G Locations: - p.Phe28Leu (Ensembl:YGL138C_mRNA) - c.82T>C (Ensembl:YGL138C_mRNA) Source type: large scale study Cross-references: - SGRP: s07-249455 | |||||||
s07-249382 | 52 | G>V | SGRP | ||||
Consequence: missense Predictions: - SIFT: tolerated - low confidence (0.12) Somatic: No Accession: VII:g.249377C>A Codon: GGT/GTT Consequence type: missense Cytogenetic band: Genomic location: VII:g.249377C>A Locations: - p.Gly52Val (Ensembl:YGL138C_mRNA) - c.155G>T (Ensembl:YGL138C_mRNA) Source type: large scale study Cross-references: - SGRP: s07-249382 | |||||||
s07-249224 | 105 | I>V | SGRP | ||||
Consequence: missense Predictions: - SIFT: tolerated (1) Somatic: No Accession: VII:g.249219T>C Codon: ATT/GTT Consequence type: missense Cytogenetic band: Genomic location: VII:g.249219T>C Locations: - p.Ile105Val (Ensembl:YGL138C_mRNA) - c.313A>G (Ensembl:YGL138C_mRNA) Source type: large scale study Cross-references: - SGRP: s07-249224 | |||||||
s07-249038 | 167 | V>L | SGRP | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.61) Somatic: No Accession: VII:g.249033C>G Codon: GTT/CTT Consequence type: missense Cytogenetic band: Genomic location: VII:g.249033C>G Locations: - p.Val167Leu (Ensembl:YGL138C_mRNA) - c.499G>C (Ensembl:YGL138C_mRNA) Source type: large scale study Cross-references: - SGRP: s07-249038 | |||||||
s07-248891 | 216 | S>T | SGRP | ||||
Consequence: missense Predictions: - SIFT: tolerated (1) Somatic: No Accession: VII:g.248886A>T Codon: TCG/ACG Consequence type: missense Cytogenetic band: Genomic location: VII:g.248886A>T Locations: - p.Ser216Thr (Ensembl:YGL138C_mRNA) - c.646T>A (Ensembl:YGL138C_mRNA) Source type: large scale study Cross-references: - SGRP: s07-248891 | |||||||
s07-248858 | 227 | L>F | SGRP | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.17) Somatic: No Accession: VII:g.248853G>A Codon: CTC/TTC Consequence type: missense Cytogenetic band: Genomic location: VII:g.248853G>A Locations: - p.Leu227Phe (Ensembl:YGL138C_mRNA) - c.679C>T (Ensembl:YGL138C_mRNA) Source type: large scale study Cross-references: - SGRP: s07-248858 | |||||||
s07-248672 | 289 | L>V | SGRP | ||||
Consequence: missense Predictions: - SIFT: tolerated - low confidence (0.41) Somatic: No Accession: VII:g.248667G>C Codon: CTA/GTA Consequence type: missense Cytogenetic band: Genomic location: VII:g.248667G>C Locations: - p.Leu289Val (Ensembl:YGL138C_mRNA) - c.865C>G (Ensembl:YGL138C_mRNA) Source type: large scale study Cross-references: - SGRP: s07-248672 | |||||||
s07-248610 | 309 | R>S | SGRP | ||||
Consequence: missense Predictions: - SIFT: tolerated - low confidence (0.27) Somatic: No Accession: VII:g.248605T>A Codon: AGA/AGT Consequence type: missense Cytogenetic band: Genomic location: VII:g.248605T>A Locations: - p.Arg309Ser (Ensembl:YGL138C_mRNA) - c.927A>T (Ensembl:YGL138C_mRNA) Source type: large scale study Cross-references: - SGRP: s07-248610 |