P46950 · SNG1_YEAST
- ProteinNitrosoguanidine resistance protein SNG1
- GeneSNG1
- StatusUniProtKB reviewed (Swiss-Prot)
- Amino acids547 (go to sequence)
- Protein existenceEvidence at protein level
- Annotation score4/5
Variants
Variant ID(s) | Position(s) | Change | Description | Clinical significance | Provenance | ||
---|---|---|---|---|---|---|---|
s07-894114 | 11 | Q>L | SGRP | ||||
Consequence: missense Predictions: - SIFT: deleterious - low confidence (0) Somatic: No Accession: VII:g.894109T>A Codon: CAG/CTG Consequence type: missense Cytogenetic band: Genomic location: VII:g.894109T>A Locations: - p.Gln11Leu (Ensembl:YGR197C_mRNA) - c.32A>T (Ensembl:YGR197C_mRNA) Source type: large scale study Cross-references: - SGRP: s07-894114 | |||||||
s07-894114 | 11 | Q>R | SGRP | ||||
Consequence: missense Predictions: - SIFT: deleterious - low confidence (0) Somatic: No Accession: VII:g.894109T>C Codon: CAG/CGG Consequence type: missense Cytogenetic band: Genomic location: VII:g.894109T>C Locations: - p.Gln11Arg (Ensembl:YGR197C_mRNA) - c.32A>G (Ensembl:YGR197C_mRNA) Source type: large scale study Cross-references: - SGRP: s07-894114 | |||||||
s07-893958 | 63 | S>C | SGRP | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.03) Somatic: No Accession: VII:g.893953G>C Codon: TCC/TGC Consequence type: missense Cytogenetic band: Genomic location: VII:g.893953G>C Locations: - p.Ser63Cys (Ensembl:YGR197C_mRNA) - c.188C>G (Ensembl:YGR197C_mRNA) Source type: large scale study Cross-references: - SGRP: s07-893958 | |||||||
s07-893734 | 138 | F>L | SGRP | ||||
Consequence: missense Predictions: - SIFT: tolerated (1) Somatic: No Accession: VII:g.893729A>G Codon: TTT/CTT Consequence type: missense Cytogenetic band: Genomic location: VII:g.893729A>G Locations: - p.Phe138Leu (Ensembl:YGR197C_mRNA) - c.412T>C (Ensembl:YGR197C_mRNA) Source type: large scale study Cross-references: - SGRP: s07-893734 | |||||||
s07-893731 | 139 | F>L | SGRP | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.4) Somatic: No Accession: VII:g.893726A>G Codon: TTC/CTC Consequence type: missense Cytogenetic band: Genomic location: VII:g.893726A>G Locations: - p.Phe139Leu (Ensembl:YGR197C_mRNA) - c.415T>C (Ensembl:YGR197C_mRNA) Source type: large scale study Cross-references: - SGRP: s07-893731 | |||||||
s07-893689 | 153 | N>D | SGRP | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.71) Somatic: No Accession: VII:g.893684T>C Codon: AAT/GAT Consequence type: missense Cytogenetic band: Genomic location: VII:g.893684T>C Locations: - p.Asn153Asp (Ensembl:YGR197C_mRNA) - c.457A>G (Ensembl:YGR197C_mRNA) Source type: large scale study Cross-references: - SGRP: s07-893689 | |||||||
s07-893648 | 166 | L>F | SGRP | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.25) Somatic: No Accession: VII:g.893643C>A Codon: TTG/TTT Consequence type: missense Cytogenetic band: Genomic location: VII:g.893643C>A Locations: - p.Leu166Phe (Ensembl:YGR197C_mRNA) - c.498G>T (Ensembl:YGR197C_mRNA) Source type: large scale study Cross-references: - SGRP: s07-893648 | |||||||
s07-893647 | 167 | L>I | SGRP | ||||
Consequence: missense Predictions: - SIFT: tolerated (1) Somatic: No Accession: VII:g.893642A>T Codon: TTA/ATA Consequence type: missense Cytogenetic band: Genomic location: VII:g.893642A>T Locations: - p.Leu167Ile (Ensembl:YGR197C_mRNA) - c.499T>A (Ensembl:YGR197C_mRNA) Source type: large scale study Cross-references: - SGRP: s07-893647 | |||||||
s07-893451 | 232 | S>W | SGRP | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.02) Somatic: No Accession: VII:g.893446G>C Codon: TCG/TGG Consequence type: missense Cytogenetic band: Genomic location: VII:g.893446G>C Locations: - p.Ser232Trp (Ensembl:YGR197C_mRNA) - c.695C>G (Ensembl:YGR197C_mRNA) Source type: large scale study Cross-references: - SGRP: s07-893451 | |||||||
s07-893434 | 238 | I>L | SGRP | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.3) Somatic: No Accession: VII:g.893429T>G Codon: ATT/CTT Consequence type: missense Cytogenetic band: Genomic location: VII:g.893429T>G Locations: - p.Ile238Leu (Ensembl:YGR197C_mRNA) - c.712A>C (Ensembl:YGR197C_mRNA) Source type: large scale study Cross-references: - SGRP: s07-893434 | |||||||
s07-893397 | 250 | P>L | SGRP | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.34) Somatic: No Accession: VII:g.893392G>A Codon: CCA/CTA Consequence type: missense Cytogenetic band: Genomic location: VII:g.893392G>A Locations: - p.Pro250Leu (Ensembl:YGR197C_mRNA) - c.749C>T (Ensembl:YGR197C_mRNA) Source type: large scale study Cross-references: - SGRP: s07-893397 | |||||||
s07-893374 | 258 | L>V | SGRP | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.19) Somatic: No Accession: VII:g.893369G>C Codon: CTA/GTA Consequence type: missense Cytogenetic band: Genomic location: VII:g.893369G>C Locations: - p.Leu258Val (Ensembl:YGR197C_mRNA) - c.772C>G (Ensembl:YGR197C_mRNA) Source type: large scale study Cross-references: - SGRP: s07-893374 | |||||||
s07-893355 | 264 | L>S | SGRP | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: VII:g.893350A>G Codon: TTG/TCG Consequence type: missense Cytogenetic band: Genomic location: VII:g.893350A>G Locations: - p.Leu264Ser (Ensembl:YGR197C_mRNA) - c.791T>C (Ensembl:YGR197C_mRNA) Source type: large scale study Cross-references: - SGRP: s07-893355 | |||||||
s07-893308 | 280 | L>M | SGRP | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.24) Somatic: No Accession: VII:g.893303A>T Codon: TTG/ATG Consequence type: missense Cytogenetic band: Genomic location: VII:g.893303A>T Locations: - p.Leu280Met (Ensembl:YGR197C_mRNA) - c.838T>A (Ensembl:YGR197C_mRNA) Source type: large scale study Cross-references: - SGRP: s07-893308 | |||||||
s07-893219 | 309 | N>K | SGRP | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.29) Somatic: No Accession: VII:g.893214G>T Codon: AAC/AAA Consequence type: missense Cytogenetic band: Genomic location: VII:g.893214G>T Locations: - p.Asn309Lys (Ensembl:YGR197C_mRNA) - c.927C>A (Ensembl:YGR197C_mRNA) Source type: large scale study Cross-references: - SGRP: s07-893219 | |||||||
s07-893208 | 313 | P>L | SGRP | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.02) Somatic: No Accession: VII:g.893203G>A Codon: CCC/CTC Consequence type: missense Cytogenetic band: Genomic location: VII:g.893203G>A Locations: - p.Pro313Leu (Ensembl:YGR197C_mRNA) - c.938C>T (Ensembl:YGR197C_mRNA) Source type: large scale study Cross-references: - SGRP: s07-893208 | |||||||
s07-893101 | 349 | A>T | SGRP | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.02) Somatic: No Accession: VII:g.893096C>T Codon: GCC/ACC Consequence type: missense Cytogenetic band: Genomic location: VII:g.893096C>T Locations: - p.Ala349Thr (Ensembl:YGR197C_mRNA) - c.1045G>A (Ensembl:YGR197C_mRNA) Source type: large scale study Cross-references: - SGRP: s07-893101 | |||||||
s07-892861 | 429 | L>M | SGRP | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.23) Somatic: No Accession: VII:g.892856G>T Codon: CTG/ATG Consequence type: missense Cytogenetic band: Genomic location: VII:g.892856G>T Locations: - p.Leu429Met (Ensembl:YGR197C_mRNA) - c.1285C>A (Ensembl:YGR197C_mRNA) Source type: large scale study Cross-references: - SGRP: s07-892861 | |||||||
s07-892819 | 443 | A>P | SGRP | ||||
Consequence: missense Predictions: - SIFT: tolerated (1) Somatic: No Accession: VII:g.892814C>G Codon: GCT/CCT Consequence type: missense Cytogenetic band: Genomic location: VII:g.892814C>G Locations: - p.Ala443Pro (Ensembl:YGR197C_mRNA) - c.1327G>C (Ensembl:YGR197C_mRNA) Source type: large scale study Cross-references: - SGRP: s07-892819 | |||||||
s07-892554 | 531 | S>N | SGRP | ||||
Consequence: missense Predictions: - SIFT: tolerated - low confidence (0.45) Somatic: No Accession: VII:g.892549C>T Codon: AGC/AAC Consequence type: missense Cytogenetic band: Genomic location: VII:g.892549C>T Locations: - p.Ser531Asn (Ensembl:YGR197C_mRNA) - c.1592G>A (Ensembl:YGR197C_mRNA) Source type: large scale study Cross-references: - SGRP: s07-892554 | |||||||
s07-892546 | 534 | A>T | SGRP | ||||
Consequence: missense Predictions: - SIFT: tolerated - low confidence (0.16) Somatic: No Accession: VII:g.892541C>T Codon: GCA/ACA Consequence type: missense Cytogenetic band: Genomic location: VII:g.892541C>T Locations: - p.Ala534Thr (Ensembl:YGR197C_mRNA) - c.1600G>A (Ensembl:YGR197C_mRNA) Source type: large scale study Cross-references: - SGRP: s07-892546 | |||||||
s07-892545 | 534 | A>V | SGRP | ||||
Consequence: missense Predictions: - SIFT: tolerated - low confidence (0.65) Somatic: No Accession: VII:g.892540G>A Codon: GCA/GTA Consequence type: missense Cytogenetic band: Genomic location: VII:g.892540G>A Locations: - p.Ala534Val (Ensembl:YGR197C_mRNA) - c.1601C>T (Ensembl:YGR197C_mRNA) Source type: large scale study Cross-references: - SGRP: s07-892545 | |||||||
s07-892527 | 540 | K>R | SGRP | ||||
Consequence: missense Somatic: No Accession: VII:g.892522T>C Codon: AAA/AGA Consequence type: missense Cytogenetic band: Genomic location: VII:g.892522T>C Locations: - p.Lys540Arg (Ensembl:YGR197C_mRNA) - c.1619A>G (Ensembl:YGR197C_mRNA) Source type: large scale study Cross-references: - SGRP: s07-892527 | |||||||
s07-892524 | 541 | N>S | SGRP | ||||
Consequence: missense Somatic: No Accession: VII:g.892519T>C Codon: AAT/AGT Consequence type: missense Cytogenetic band: Genomic location: VII:g.892519T>C Locations: - p.Asn541Ser (Ensembl:YGR197C_mRNA) - c.1622A>G (Ensembl:YGR197C_mRNA) Source type: large scale study Cross-references: - SGRP: s07-892524 |