A0A1W2P7M3 · A0A1W2P7M3_MOUSE
- ProteinRIKEN cDNA 2610008E11 gene
- Gene2610008E11Rik
- StatusUniProtKB unreviewed (TrEMBL)
- Organism
- Amino acids194 (go to sequence)
- Protein existenceInferred from homology
- Annotation score1/5
Variants
Variant ID(s) | Position(s) | Change | Description | Clinical significance | Provenance | ||
---|---|---|---|---|---|---|---|
rs3389110626 | 18 | F>S | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.07) Somatic: No Accession: NC_000076.7:g.78930360A>G Codon: TTC/TCC Consequence type: missense Cytogenetic band: 10q Genomic location: NC_000076.7:g.78930360A>G Locations: - p.Phe18Ser (Ensembl:ENSMUST00000218854) - c.53T>C (Ensembl:ENSMUST00000218854) Source type: large scale study Cross-references: | |||||||
rs864277856 | 21 | W>R | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.12) Somatic: No Accession: NC_000076.7:g.78930352A>G Codon: TGG/CGG Consequence type: missense Cytogenetic band: 10q Genomic location: NC_000076.7:g.78930352A>G Locations: - p.Trp21Arg (Ensembl:ENSMUST00000218854) - c.61T>C (Ensembl:ENSMUST00000218854) Source type: large scale study Cross-references: | |||||||
rs3389121638 | 39 | M>I | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: NC_000076.7:g.78930296C>A Codon: ATG/ATT Consequence type: missense Cytogenetic band: 10q Genomic location: NC_000076.7:g.78930296C>A Locations: - p.Met39Ile (Ensembl:ENSMUST00000218854) - c.117G>T (Ensembl:ENSMUST00000218854) Source type: large scale study Cross-references: | |||||||
rs218084228 | 44 | S>N | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.1) Somatic: No Accession: NC_000076.7:g.78930282C>T Codon: AGT/AAT Consequence type: missense Cytogenetic band: 10q Genomic location: NC_000076.7:g.78930282C>T Locations: - p.Ser44Asn (Ensembl:ENSMUST00000218854) - c.131G>A (Ensembl:ENSMUST00000218854) Source type: large scale study Cross-references: | |||||||
rs3400203079 | 78 | N>M | EVA | ||||
Consequence: stop gained Somatic: No Accession: NC_000076.7:g.78928255_78928256insAGTGCAT Codon: AAC/ATGCACTAAC Consequence type: stop gained Cytogenetic band: 10q Genomic location: NC_000076.7:g.78928255_78928256insAGTGCAT Locations: - p.Asn78MetfsTer3 (Ensembl:ENSMUST00000218854) - c.232_233insTGCACTA (Ensembl:ENSMUST00000218854) Source type: large scale study Cross-references: | |||||||
rs263278954 | 102 | G>R | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.52) Somatic: No Accession: NC_000076.7:g.78924151C>G Codon: GGC/CGC Consequence type: missense Cytogenetic band: 10q Genomic location: NC_000076.7:g.78924151C>G Locations: - p.Gly102Arg (Ensembl:ENSMUST00000218854) - c.304G>C (Ensembl:ENSMUST00000218854) Source type: large scale study Cross-references: | |||||||
rs249159069 | 108 | W>C | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.22) Somatic: No Accession: NC_000076.7:g.78924131C>A Codon: TGG/TGT Consequence type: missense Cytogenetic band: 10q Genomic location: NC_000076.7:g.78924131C>A Locations: - p.Trp108Cys (Ensembl:ENSMUST00000218854) - c.324G>T (Ensembl:ENSMUST00000218854) Source type: large scale study Cross-references: | |||||||
rs45738920 | 115 | K>N | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.13) Somatic: No Accession: NC_000076.7:g.78904552C>A Codon: AAG/AAT Consequence type: missense Cytogenetic band: 10q Genomic location: NC_000076.7:g.78904552C>A Locations: - p.Lys115Asn (Ensembl:ENSMUST00000218854) - c.345G>T (Ensembl:ENSMUST00000218854) Source type: large scale study Cross-references: | |||||||
rs51786549 | 135 | D>E | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (1) Somatic: No Accession: NC_000076.7:g.78903826A>T Codon: GAT/GAA Consequence type: missense Cytogenetic band: 10q Genomic location: NC_000076.7:g.78903826A>T Locations: - p.Asp135Glu (Ensembl:ENSMUST00000218854) - c.405T>A (Ensembl:ENSMUST00000218854) Source type: large scale study Cross-references: | |||||||
rs252127690 | 140 | F>L | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.41) Somatic: No Accession: NC_000076.7:g.78903811A>T Codon: TTT/TTA Consequence type: missense Cytogenetic band: 10q Genomic location: NC_000076.7:g.78903811A>T Locations: - p.Phe140Leu (Ensembl:ENSMUST00000218854) - c.420T>A (Ensembl:ENSMUST00000218854) Source type: large scale study Cross-references: |