Q62384 · ZPR1_MOUSE
- ProteinZinc finger protein ZPR1
- GeneZpr1
- StatusUniProtKB reviewed (Swiss-Prot)
- Organism
- Amino acids459 (go to sequence)
- Protein existenceEvidence at protein level
- Annotation score5/5
Variants
Variant ID(s) | Position(s) | Change | Description | Clinical significance | Provenance | ||
---|---|---|---|---|---|---|---|
rs51304513 | 18 | P>S | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated - low confidence (0.09) Somatic: No Accession: NC_000075.7:g.46184546C>T Codon: CCC/TCC Consequence type: missense Cytogenetic band: 9q Genomic location: NC_000075.7:g.46184546C>T Locations: - p.Pro18Ser (Ensembl:ENSMUST00000156440) - c.52C>T (Ensembl:ENSMUST00000156440) Source type: large scale study Cross-references: | |||||||
rs3389036515 | 27 | A>V | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.31) Somatic: No Accession: NC_000075.7:g.46184574C>T Codon: GCC/GTC Consequence type: missense Cytogenetic band: 9q Genomic location: NC_000075.7:g.46184574C>T Locations: - p.Ala27Val (Ensembl:ENSMUST00000156440) - c.80C>T (Ensembl:ENSMUST00000156440) Source type: large scale study Cross-references: | |||||||
rs3400080539 | 37 | A>P | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.04) Somatic: No Accession: NC_000075.7:g.46184603G>C Codon: GCC/CCC Consequence type: missense Cytogenetic band: 9q Genomic location: NC_000075.7:g.46184603G>C Locations: - p.Ala37Pro (Ensembl:ENSMUST00000156440) - c.109G>C (Ensembl:ENSMUST00000156440) Source type: large scale study Cross-references: | |||||||
rs3389009444 | 113 | M>V | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.02) Somatic: No Accession: NC_000075.7:g.46185357A>G Codon: ATG/GTG Consequence type: missense Cytogenetic band: 9q Genomic location: NC_000075.7:g.46185357A>G Locations: - p.Met113Val (Ensembl:ENSMUST00000156440) - c.337A>G (Ensembl:ENSMUST00000156440) Source type: large scale study Cross-references: | |||||||
rs3389045436 | 132 | F>Y | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: NC_000075.7:g.46185415T>A Codon: TTT/TAT Consequence type: missense Cytogenetic band: 9q Genomic location: NC_000075.7:g.46185415T>A Locations: - p.Phe132Tyr (Ensembl:ENSMUST00000156440) - c.395T>A (Ensembl:ENSMUST00000156440) Source type: large scale study Cross-references: | |||||||
rs248687140 | 177 | E>A | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.23) Somatic: No Accession: NC_000075.7:g.46186696A>C Codon: GAG/GCG Consequence type: missense Cytogenetic band: 9q Genomic location: NC_000075.7:g.46186696A>C Locations: - p.Glu177Ala (Ensembl:ENSMUST00000156440) - c.530A>C (Ensembl:ENSMUST00000156440) Source type: large scale study Cross-references: | |||||||
rs1134547640 | 207 | N>K | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: NC_000075.7:g.46187067C>G Codon: AAC/AAG Consequence type: missense Cytogenetic band: 9q Genomic location: NC_000075.7:g.46187067C>G Locations: - p.Asn207Lys (Ensembl:ENSMUST00000156440) - c.621C>G (Ensembl:ENSMUST00000156440) Source type: large scale study Cross-references: | |||||||
rs3389030093 | 209 | H>L | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.46) Somatic: No Accession: NC_000075.7:g.46187072A>T Codon: CAT/CTT Consequence type: missense Cytogenetic band: 9q Genomic location: NC_000075.7:g.46187072A>T Locations: - p.His209Leu (Ensembl:ENSMUST00000156440) - c.626A>T (Ensembl:ENSMUST00000156440) Source type: large scale study Cross-references: | |||||||
rs234150434 | 209 | H>Q | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.25) Somatic: No Accession: NC_000075.7:g.46187073T>A Codon: CAT/CAA Consequence type: missense Cytogenetic band: 9q Genomic location: NC_000075.7:g.46187073T>A Locations: - p.His209Gln (Ensembl:ENSMUST00000156440) - c.627T>A (Ensembl:ENSMUST00000156440) Source type: large scale study Cross-references: | |||||||
rs13466235 | 262 | C>R | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: NC_000075.7:g.46187740T>C Codon: TGC/CGC Consequence type: missense Cytogenetic band: 9q Genomic location: NC_000075.7:g.46187740T>C Locations: - p.Cys262Arg (Ensembl:ENSMUST00000156440) - c.784T>C (Ensembl:ENSMUST00000156440) Source type: large scale study Cross-references: | |||||||
rs3389009430 | 264 | A>S | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.23) Somatic: No Accession: NC_000075.7:g.46187746G>T Codon: GCT/TCT Consequence type: missense Cytogenetic band: 9q Genomic location: NC_000075.7:g.46187746G>T Locations: - p.Ala264Ser (Ensembl:ENSMUST00000156440) - c.790G>T (Ensembl:ENSMUST00000156440) Source type: large scale study Cross-references: | |||||||
rs3389015595 | 317 | D>G | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.24) Somatic: No Accession: NC_000075.7:g.46189002A>G Codon: GAT/GGT Consequence type: missense Cytogenetic band: 9q Genomic location: NC_000075.7:g.46189002A>G Locations: - p.Asp317Gly (Ensembl:ENSMUST00000156440) - c.950A>G (Ensembl:ENSMUST00000156440) Source type: large scale study Cross-references: | |||||||
rs3410464777 | 319 | S>L | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.08) Somatic: No Accession: NC_000075.7:g.46189008C>T Codon: TCA/TTA Consequence type: missense Cytogenetic band: 9q Genomic location: NC_000075.7:g.46189008C>T Locations: - p.Ser319Leu (Ensembl:ENSMUST00000156440) - c.956C>T (Ensembl:ENSMUST00000156440) Source type: large scale study Cross-references: | |||||||
rs3389039228 | 350 | K>N | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.02) Somatic: No Accession: NC_000075.7:g.46189670G>T Codon: AAG/AAT Consequence type: missense Cytogenetic band: 9q Genomic location: NC_000075.7:g.46189670G>T Locations: - p.Lys350Asn (Ensembl:ENSMUST00000156440) - c.1050G>T (Ensembl:ENSMUST00000156440) Source type: large scale study Cross-references: | |||||||
rs3389045454 | 360 | D>E | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.04) Somatic: No Accession: NC_000075.7:g.46189700C>G Codon: GAC/GAG Consequence type: missense Cytogenetic band: 9q Genomic location: NC_000075.7:g.46189700C>G Locations: - p.Asp360Glu (Ensembl:ENSMUST00000156440) - c.1080C>G (Ensembl:ENSMUST00000156440) Source type: large scale study Cross-references: | |||||||
rs3389040948 | 376 | S>F | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.01) Somatic: No Accession: NC_000075.7:g.46191001C>T Codon: TCT/TTT Consequence type: missense Cytogenetic band: 9q Genomic location: NC_000075.7:g.46191001C>T Locations: - p.Ser376Phe (Ensembl:ENSMUST00000156440) - c.1127C>T (Ensembl:ENSMUST00000156440) Source type: large scale study Cross-references: | |||||||
rs3389047110 | 397 | G>S | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.04) Somatic: No Accession: NC_000075.7:g.46191223G>A Codon: GGC/AGC Consequence type: missense Cytogenetic band: 9q Genomic location: NC_000075.7:g.46191223G>A Locations: - p.Gly397Ser (Ensembl:ENSMUST00000156440) - c.1189G>A (Ensembl:ENSMUST00000156440) Source type: large scale study Cross-references: | |||||||
rs3389021266 | 449 | E>D | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.05) Somatic: No Accession: NC_000075.7:g.46192437G>T Codon: GAG/GAT Consequence type: missense Cytogenetic band: 9q Genomic location: NC_000075.7:g.46192437G>T Locations: - p.Glu449Asp (Ensembl:ENSMUST00000156440) - c.1347G>T (Ensembl:ENSMUST00000156440) Source type: large scale study Cross-references: |