Q8VEG6 · CNO6L_MOUSE
- ProteinCCR4-NOT transcription complex subunit 6-like
- GeneCnot6l
- StatusUniProtKB reviewed (Swiss-Prot)
- Organism
- Amino acids555 (go to sequence)
- Protein existenceEvidence at protein level
- Annotation score5/5
Variants
Variant ID(s) | Position(s) | Change | Description | Clinical significance | Provenance | ||
---|---|---|---|---|---|---|---|
rs3388743537 | 4 | I>T | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated - low confidence (0.46) Somatic: No Accession: NC_000071.7:g.96281986A>G Codon: ATA/ACA Consequence type: missense Cytogenetic band: 5q Genomic location: NC_000071.7:g.96281986A>G Locations: - p.Ile4Thr (Ensembl:ENSMUST00000113005) - c.11T>C (Ensembl:ENSMUST00000113005) Source type: large scale study Cross-references: | |||||||
rs3388757620 | 33 | K>N | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.02) Somatic: No Accession: NC_000071.7:g.96281898T>A Codon: AAA/AAT Consequence type: missense Cytogenetic band: 5q Genomic location: NC_000071.7:g.96281898T>A Locations: - p.Lys33Asn (Ensembl:ENSMUST00000113005) - c.99A>T (Ensembl:ENSMUST00000113005) Source type: large scale study Cross-references: | |||||||
rs3388774501 | 44 | R>S | EVA | ||||
Consequence: stop gained Somatic: No Accession: NC_000071.7:g.96279100_96279101insACCTCAACCATCACTCA Codon: AGA/AGTGAGTGATGGTTGAGGTA Consequence type: stop gained Cytogenetic band: 5q Genomic location: NC_000071.7:g.96279100_96279101insACCTCAACCATCACTCA Locations: - p.Arg44SerfsTer3 (Ensembl:ENSMUST00000113005) - c.131_132insTGAGTGATGGTTGAGGT (Ensembl:ENSMUST00000113005) Source type: large scale study Cross-references: | |||||||
rs3388771450 | 46 | R>W | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: NC_000071.7:g.96279096G>A Codon: CGG/TGG Consequence type: missense Cytogenetic band: 5q Genomic location: NC_000071.7:g.96279096G>A Locations: - p.Arg46Trp (Ensembl:ENSMUST00000113005) - c.136C>T (Ensembl:ENSMUST00000113005) Source type: large scale study Cross-references: | |||||||
rs3388778609 | 62 | H>R | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.01) Somatic: No Accession: NC_000071.7:g.96279047T>C Codon: CAC/CGC Consequence type: missense Cytogenetic band: 5q Genomic location: NC_000071.7:g.96279047T>C Locations: - p.His62Arg (Ensembl:ENSMUST00000113005) - c.185A>G (Ensembl:ENSMUST00000113005) Source type: large scale study Cross-references: | |||||||
rs3388743451 | 67 | N>Y | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.52) Somatic: No Accession: NC_000071.7:g.96279033T>A Codon: AAC/TAC Consequence type: missense Cytogenetic band: 5q Genomic location: NC_000071.7:g.96279033T>A Locations: - p.Asn67Tyr (Ensembl:ENSMUST00000113005) - c.199A>T (Ensembl:ENSMUST00000113005) Source type: large scale study Cross-references: | |||||||
rs3388778598 | 69 | A>G | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.01) Somatic: No Accession: NC_000071.7:g.96279026G>C Codon: GCT/GGT Consequence type: missense Cytogenetic band: 5q Genomic location: NC_000071.7:g.96279026G>C Locations: - p.Ala69Gly (Ensembl:ENSMUST00000113005) - c.206C>G (Ensembl:ENSMUST00000113005) Source type: large scale study Cross-references: | |||||||
rs3388760361 | 69 | A>T | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.77) Somatic: No Accession: NC_000071.7:g.96279027C>T Codon: GCT/ACT Consequence type: missense Cytogenetic band: 5q Genomic location: NC_000071.7:g.96279027C>T Locations: - p.Ala69Thr (Ensembl:ENSMUST00000113005) - c.205G>A (Ensembl:ENSMUST00000113005) Source type: large scale study Cross-references: | |||||||
rs3388765239 | 237 | S>N | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.04) Somatic: No Accession: NC_000071.7:g.96242027C>T Codon: AGT/AAT Consequence type: missense Cytogenetic band: 5q Genomic location: NC_000071.7:g.96242027C>T Locations: - p.Ser237Asn (Ensembl:ENSMUST00000113005) - c.710G>A (Ensembl:ENSMUST00000113005) Source type: large scale study Cross-references: | |||||||
rs3388768728 | 291 | K>N | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: NC_000071.7:g.96234152T>A Codon: AAA/AAT Consequence type: missense Cytogenetic band: 5q Genomic location: NC_000071.7:g.96234152T>A Locations: - p.Lys291Asn (Ensembl:ENSMUST00000113005) - c.873A>T (Ensembl:ENSMUST00000113005) Source type: large scale study Cross-references: | |||||||
rs3388767181 | 383 | K>I | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: NC_000071.7:g.96230833T>A Codon: AAA/ATA Consequence type: missense Cytogenetic band: 5q Genomic location: NC_000071.7:g.96230833T>A Locations: - p.Lys383Ile (Ensembl:ENSMUST00000113005) - c.1148A>T (Ensembl:ENSMUST00000113005) Source type: large scale study Cross-references: | |||||||
rs3388772476 | 419 | V>* | EVA | ||||
Consequence: stop gained Somatic: No Accession: NC_000071.7:g.96227992_96227993insCTCA Codon: -/TGAG Consequence type: stop gained Cytogenetic band: 5q Genomic location: NC_000071.7:g.96227992_96227993insCTCA Locations: - p.Val419Ter (Ensembl:ENSMUST00000113005) - c.1254_1255insTGAG (Ensembl:ENSMUST00000113005) Source type: large scale study Cross-references: | |||||||
rs3388767188 | 524 | H>Y | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.03) Somatic: No Accession: NC_000071.7:g.96225137G>A Codon: CAC/TAC Consequence type: missense Cytogenetic band: 5q Genomic location: NC_000071.7:g.96225137G>A Locations: - p.His524Tyr (Ensembl:ENSMUST00000113005) - c.1570C>T (Ensembl:ENSMUST00000113005) Source type: large scale study Cross-references: | |||||||
rs3388765834 | 526 | P>S | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.02) Somatic: No Accession: NC_000071.7:g.96225131G>A Codon: CCT/TCT Consequence type: missense Cytogenetic band: 5q Genomic location: NC_000071.7:g.96225131G>A Locations: - p.Pro526Ser (Ensembl:ENSMUST00000113005) - c.1576C>T (Ensembl:ENSMUST00000113005) Source type: large scale study Cross-references: | |||||||
rs3388743469 | 536 | L>F | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.4) Somatic: No Accession: NC_000071.7:g.96225101G>A Codon: CTT/TTT Consequence type: missense Cytogenetic band: 5q Genomic location: NC_000071.7:g.96225101G>A Locations: - p.Leu536Phe (Ensembl:ENSMUST00000113005) - c.1606C>T (Ensembl:ENSMUST00000113005) Source type: large scale study Cross-references: | |||||||
rs3543623867 | 539 | H>P | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.21) Somatic: No Accession: NC_000071.7:g.96225091T>G Codon: CAC/CCC Consequence type: missense Cytogenetic band: 5q Genomic location: NC_000071.7:g.96225091T>G Locations: - p.His539Pro (Ensembl:ENSMUST00000113005) - c.1616A>C (Ensembl:ENSMUST00000113005) Source type: large scale study Cross-references: |