Q5QD16 · TAAR3_MOUSE
- ProteinTrace amine-associated receptor 3
- GeneTaar3
- StatusUniProtKB reviewed (Swiss-Prot)
- Organism
- Amino acids343 (go to sequence)
- Protein existenceEvidence at transcript level
- Annotation score4/5
Variants
Variant ID(s) | Position(s) | Change | Description | Clinical significance | Provenance | ||
---|---|---|---|---|---|---|---|
rs3389065924 | 15 | K>R | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.03) Somatic: No Accession: NC_000076.7:g.23825499A>G Codon: AAA/AGA Consequence type: missense Cytogenetic band: 10q Genomic location: NC_000076.7:g.23825499A>G Locations: - p.Lys15Arg (Ensembl:ENSMUST00000045152) - c.44A>G (Ensembl:ENSMUST00000045152) Source type: large scale study Cross-references: | |||||||
rs3389065978 | 34 | M>I | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.07) Somatic: No Accession: NC_000076.7:g.23825557G>A Codon: ATG/ATA Consequence type: missense Cytogenetic band: 10q Genomic location: NC_000076.7:g.23825557G>A Locations: - p.Met34Ile (Ensembl:ENSMUST00000045152) - c.102G>A (Ensembl:ENSMUST00000045152) Source type: large scale study Cross-references: | |||||||
rs3389091646 | 34 | M>K | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.01) Somatic: No Accession: NC_000076.7:g.23825556T>A Codon: ATG/AAG Consequence type: missense Cytogenetic band: 10q Genomic location: NC_000076.7:g.23825556T>A Locations: - p.Met34Lys (Ensembl:ENSMUST00000045152) - c.101T>A (Ensembl:ENSMUST00000045152) Source type: large scale study Cross-references: | |||||||
rs3389094200 | 45 | T>N | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: NC_000076.7:g.23825589C>A Codon: ACC/AAC Consequence type: missense Cytogenetic band: 10q Genomic location: NC_000076.7:g.23825589C>A Locations: - p.Thr45Asn (Ensembl:ENSMUST00000045152) - c.134C>A (Ensembl:ENSMUST00000045152) Source type: large scale study Cross-references: | |||||||
rs3400974362 | 46 | I>M | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.42) Somatic: No Accession: NC_000076.7:g.23825593C>G Codon: ATC/ATG Consequence type: missense Cytogenetic band: 10q Genomic location: NC_000076.7:g.23825593C>G Locations: - p.Ile46Met (Ensembl:ENSMUST00000045152) - c.138C>G (Ensembl:ENSMUST00000045152) Source type: large scale study Cross-references: | |||||||
rs3400386661 | 46 | I>N | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: NC_000076.7:g.23825592T>A Codon: ATC/AAC Consequence type: missense Cytogenetic band: 10q Genomic location: NC_000076.7:g.23825592T>A Locations: - p.Ile46Asn (Ensembl:ENSMUST00000045152) - c.137T>A (Ensembl:ENSMUST00000045152) Source type: large scale study Cross-references: | |||||||
rs3400974311 | 48 | G>A | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: NC_000076.7:g.23825598G>C Codon: GGA/GCA Consequence type: missense Cytogenetic band: 10q Genomic location: NC_000076.7:g.23825598G>C Locations: - p.Gly48Ala (Ensembl:ENSMUST00000045152) - c.143G>C (Ensembl:ENSMUST00000045152) Source type: large scale study Cross-references: | |||||||
rs3399873967 | 48 | G>R | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: NC_000076.7:g.23825597G>C Codon: GGA/CGA Consequence type: missense Cytogenetic band: 10q Genomic location: NC_000076.7:g.23825597G>C Locations: - p.Gly48Arg (Ensembl:ENSMUST00000045152) - c.142G>C (Ensembl:ENSMUST00000045152) Source type: large scale study Cross-references: | |||||||
rs3400876365 | 50 | L>F | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.02) Somatic: No Accession: NC_000076.7:g.23825605A>T Codon: TTA/TTT Consequence type: missense Cytogenetic band: 10q Genomic location: NC_000076.7:g.23825605A>T Locations: - p.Leu50Phe (Ensembl:ENSMUST00000045152) - c.150A>T (Ensembl:ENSMUST00000045152) Source type: large scale study Cross-references: | |||||||
rs3401249480 | 50 | L>I | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.02) Somatic: No Accession: NC_000076.7:g.23825603T>A Codon: TTA/ATA Consequence type: missense Cytogenetic band: 10q Genomic location: NC_000076.7:g.23825603T>A Locations: - p.Leu50Ile (Ensembl:ENSMUST00000045152) - c.148T>A (Ensembl:ENSMUST00000045152) Source type: large scale study Cross-references: | |||||||
rs3389091777 | 52 | I>M | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.13) Somatic: No Accession: NC_000076.7:g.23825611A>G Codon: ATA/ATG Consequence type: missense Cytogenetic band: 10q Genomic location: NC_000076.7:g.23825611A>G Locations: - p.Ile52Met (Ensembl:ENSMUST00000045152) - c.156A>G (Ensembl:ENSMUST00000045152) Source type: large scale study Cross-references: | |||||||
rs3389091980 | 58 | H>L | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.04) Somatic: No Accession: NC_000076.7:g.23825628A>T Codon: CAT/CTT Consequence type: missense Cytogenetic band: 10q Genomic location: NC_000076.7:g.23825628A>T Locations: - p.His58Leu (Ensembl:ENSMUST00000045152) - c.173A>T (Ensembl:ENSMUST00000045152) Source type: large scale study Cross-references: | |||||||
rs3389091639 | 67 | N>K | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: NC_000076.7:g.23825656C>A Codon: AAC/AAA Consequence type: missense Cytogenetic band: 10q Genomic location: NC_000076.7:g.23825656C>A Locations: - p.Asn67Lys (Ensembl:ENSMUST00000045152) - c.201C>A (Ensembl:ENSMUST00000045152) Source type: large scale study Cross-references: | |||||||
rs3389102469 | 74 | A>V | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.03) Somatic: No Accession: NC_000076.7:g.23825676C>T Codon: GCA/GTA Consequence type: missense Cytogenetic band: 10q Genomic location: NC_000076.7:g.23825676C>T Locations: - p.Ala74Val (Ensembl:ENSMUST00000045152) - c.221C>T (Ensembl:ENSMUST00000045152) Source type: large scale study Cross-references: | |||||||
rs3389084839 | 103 | F>L | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.03) Somatic: No Accession: NC_000076.7:g.23825764T>A Codon: TTT/TTA Consequence type: missense Cytogenetic band: 10q Genomic location: NC_000076.7:g.23825764T>A Locations: - p.Phe103Leu (Ensembl:ENSMUST00000045152) - c.309T>A (Ensembl:ENSMUST00000045152) Source type: large scale study Cross-references: | |||||||
rs3389088728 | 104 | C>R | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.01) Somatic: No Accession: NC_000076.7:g.23825765T>C Codon: TGC/CGC Consequence type: missense Cytogenetic band: 10q Genomic location: NC_000076.7:g.23825765T>C Locations: - p.Cys104Arg (Ensembl:ENSMUST00000045152) - c.310T>C (Ensembl:ENSMUST00000045152) Source type: large scale study Cross-references: | |||||||
rs3547729396 | 108 | A>T | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (1) Somatic: No Accession: NC_000076.7:g.23825777G>A Codon: GCG/ACG Consequence type: missense Cytogenetic band: 10q Genomic location: NC_000076.7:g.23825777G>A Locations: - p.Ala108Thr (Ensembl:ENSMUST00000045152) - c.322G>A (Ensembl:ENSMUST00000045152) Source type: large scale study Cross-references: | |||||||
rs3389079503 | 148 | I>N | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: NC_000076.7:g.23825898T>A Codon: ATC/AAC Consequence type: missense Cytogenetic band: 10q Genomic location: NC_000076.7:g.23825898T>A Locations: - p.Ile148Asn (Ensembl:ENSMUST00000045152) - c.443T>A (Ensembl:ENSMUST00000045152) Source type: large scale study Cross-references: | |||||||
rs3389091595 | 153 | A>T | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.4) Somatic: No Accession: NC_000076.7:g.23825912G>A Codon: GCT/ACT Consequence type: missense Cytogenetic band: 10q Genomic location: NC_000076.7:g.23825912G>A Locations: - p.Ala153Thr (Ensembl:ENSMUST00000045152) - c.457G>A (Ensembl:ENSMUST00000045152) Source type: large scale study Cross-references: | |||||||
rs3389084789 | 204 | T>N | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: NC_000076.7:g.23826066C>A Codon: ACC/AAC Consequence type: missense Cytogenetic band: 10q Genomic location: NC_000076.7:g.23826066C>A Locations: - p.Thr204Asn (Ensembl:ENSMUST00000045152) - c.611C>A (Ensembl:ENSMUST00000045152) Source type: large scale study Cross-references: | |||||||
rs3389035405 | 234 | M>V | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.55) Somatic: No Accession: NC_000076.7:g.23826155A>G Codon: ATG/GTG Consequence type: missense Cytogenetic band: 10q Genomic location: NC_000076.7:g.23826155A>G Locations: - p.Met234Val (Ensembl:ENSMUST00000045152) - c.700A>G (Ensembl:ENSMUST00000045152) Source type: large scale study Cross-references: | |||||||
rs3389091832 | 241 | A>T | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.38) Somatic: No Accession: NC_000076.7:g.23826176G>A Codon: GCA/ACA Consequence type: missense Cytogenetic band: 10q Genomic location: NC_000076.7:g.23826176G>A Locations: - p.Ala241Thr (Ensembl:ENSMUST00000045152) - c.721G>A (Ensembl:ENSMUST00000045152) Source type: large scale study Cross-references: | |||||||
rs3547729418 | 299 | Y>D | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: NC_000076.7:g.23826350T>G Codon: TAC/GAC Consequence type: missense Cytogenetic band: 10q Genomic location: NC_000076.7:g.23826350T>G Locations: - p.Tyr299Asp (Ensembl:ENSMUST00000045152) - c.895T>G (Ensembl:ENSMUST00000045152) Source type: large scale study Cross-references: | |||||||
rs3389094056 | 321 | Q>H | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.02) Somatic: No Accession: NC_000076.7:g.23826418G>C Codon: CAG/CAC Consequence type: missense Cytogenetic band: 10q Genomic location: NC_000076.7:g.23826418G>C Locations: - p.Gln321His (Ensembl:ENSMUST00000045152) - c.963G>C (Ensembl:ENSMUST00000045152) Source type: large scale study Cross-references: | |||||||
rs3401059567 | 328 | I>R | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: NC_000076.7:g.23826438T>G Codon: ATA/AGA Consequence type: missense Cytogenetic band: 10q Genomic location: NC_000076.7:g.23826438T>G Locations: - p.Ile328Arg (Ensembl:ENSMUST00000045152) - c.983T>G (Ensembl:ENSMUST00000045152) Source type: large scale study Cross-references: |