A0A0R4J212 · A0A0R4J212_MOUSE
- ProteinNeural precursor cell expressed, developmentally down-regulated gene 9
- GeneNedd9
- StatusUniProtKB unreviewed (TrEMBL)
- Organism
- Amino acids833 (go to sequence)
- Protein existenceEvidence at protein level
- Annotation score2/5
Variants
Variant ID(s) | Position(s) | Change | Description | Clinical significance | Provenance | ||
---|---|---|---|---|---|---|---|
rs3389291335 | 27 | G>E | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: NC_000079.7:g.41492429C>T Codon: GGA/GAA Consequence type: missense Cytogenetic band: 13q Genomic location: NC_000079.7:g.41492429C>T Locations: - p.Gly27Glu (Ensembl:ENSMUST00000163623) - c.80G>A (Ensembl:ENSMUST00000163623) Source type: large scale study Cross-references: | |||||||
rs3389279155 | 52 | Q>* | EVA | ||||
Consequence: stop gained Somatic: No Accession: NC_000079.7:g.41492355G>A Codon: CAA/TAA Consequence type: stop gained Cytogenetic band: 13q Genomic location: NC_000079.7:g.41492355G>A Locations: - p.Gln52Ter (Ensembl:ENSMUST00000163623) - c.154C>T (Ensembl:ENSMUST00000163623) Source type: large scale study Cross-references: | |||||||
rs3550098422 | 64 | I>V | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.67) Somatic: No Accession: NC_000079.7:g.41492319T>C Codon: ATT/GTT Consequence type: missense Cytogenetic band: 13q Genomic location: NC_000079.7:g.41492319T>C Locations: - p.Ile64Val (Ensembl:ENSMUST00000163623) - c.190A>G (Ensembl:ENSMUST00000163623) Source type: large scale study Cross-references: | |||||||
rs3389237118 | 79 | G>A | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.63) Somatic: No Accession: NC_000079.7:g.41492273C>G Codon: GGA/GCA Consequence type: missense Cytogenetic band: 13q Genomic location: NC_000079.7:g.41492273C>G Locations: - p.Gly79Ala (Ensembl:ENSMUST00000163623) - c.236G>C (Ensembl:ENSMUST00000163623) Source type: large scale study Cross-references: | |||||||
rs3389263661 | 106 | Q>R | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: NC_000079.7:g.41492192T>C Codon: CAA/CGA Consequence type: missense Cytogenetic band: 13q Genomic location: NC_000079.7:g.41492192T>C Locations: - p.Gln106Arg (Ensembl:ENSMUST00000163623) - c.317A>G (Ensembl:ENSMUST00000163623) Source type: large scale study Cross-references: | |||||||
rs233904138 | 161 | H>Q | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (1) Somatic: No Accession: NC_000079.7:g.41471995A>C Codon: CAT/CAG Consequence type: missense Cytogenetic band: 13q Genomic location: NC_000079.7:g.41471995A>C Locations: - p.His161Gln (Ensembl:ENSMUST00000163623) - c.483T>G (Ensembl:ENSMUST00000163623) Source type: large scale study Cross-references: | |||||||
rs3389287485 | 167 | Y>H | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.53) Somatic: No Accession: NC_000079.7:g.41471979A>G Codon: TAC/CAC Consequence type: missense Cytogenetic band: 13q Genomic location: NC_000079.7:g.41471979A>G Locations: - p.Tyr167His (Ensembl:ENSMUST00000163623) - c.499T>C (Ensembl:ENSMUST00000163623) Source type: large scale study Cross-references: | |||||||
rs3389246366 | 170 | R>I | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.07) Somatic: No Accession: NC_000079.7:g.41471969C>A Codon: AGA/ATA Consequence type: missense Cytogenetic band: 13q Genomic location: NC_000079.7:g.41471969C>A Locations: - p.Arg170Ile (Ensembl:ENSMUST00000163623) - c.509G>T (Ensembl:ENSMUST00000163623) Source type: large scale study Cross-references: | |||||||
rs3389273019 | 172 | Q>K | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.01) Somatic: No Accession: NC_000079.7:g.41471964G>T Codon: CAA/AAA Consequence type: missense Cytogenetic band: 13q Genomic location: NC_000079.7:g.41471964G>T Locations: - p.Gln172Lys (Ensembl:ENSMUST00000163623) - c.514C>A (Ensembl:ENSMUST00000163623) Source type: large scale study Cross-references: | |||||||
rs3389253325 | 175 | V>A | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.15) Somatic: No Accession: NC_000079.7:g.41471954A>G Codon: GTC/GCC Consequence type: missense Cytogenetic band: 13q Genomic location: NC_000079.7:g.41471954A>G Locations: - p.Val175Ala (Ensembl:ENSMUST00000163623) - c.524T>C (Ensembl:ENSMUST00000163623) Source type: large scale study Cross-references: | |||||||
rs3389263604 | 180 | P>A | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.03) Somatic: No Accession: NC_000079.7:g.41471940G>C Codon: CCT/GCT Consequence type: missense Cytogenetic band: 13q Genomic location: NC_000079.7:g.41471940G>C Locations: - p.Pro180Ala (Ensembl:ENSMUST00000163623) - c.538C>G (Ensembl:ENSMUST00000163623) Source type: large scale study Cross-references: | |||||||
rs3389279187 | 212 | V>L | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.13) Somatic: No Accession: NC_000079.7:g.41471364C>A Codon: GTA/TTA Consequence type: missense Cytogenetic band: 13q Genomic location: NC_000079.7:g.41471364C>A Locations: - p.Val212Leu (Ensembl:ENSMUST00000163623) - c.634G>T (Ensembl:ENSMUST00000163623) Source type: large scale study Cross-references: | |||||||
rs3389275441 | 310 | D>N | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.18) Somatic: No Accession: NC_000079.7:g.41470224C>T Codon: GAC/AAC Consequence type: missense Cytogenetic band: 13q Genomic location: NC_000079.7:g.41470224C>T Locations: - p.Asp310Asn (Ensembl:ENSMUST00000163623) - c.928G>A (Ensembl:ENSMUST00000163623) Source type: large scale study Cross-references: | |||||||
rs1132041282 | 313 | S>N | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.42) Somatic: No Accession: NC_000079.7:g.41470214C>T Codon: AGT/AAT Consequence type: missense Cytogenetic band: 13q Genomic location: NC_000079.7:g.41470214C>T Locations: - p.Ser313Asn (Ensembl:ENSMUST00000163623) - c.938G>A (Ensembl:ENSMUST00000163623) Source type: large scale study Cross-references: | |||||||
rs3404006780 | 326 | E>* | EVA | ||||
Consequence: stop gained Somatic: No Accession: NC_000079.7:g.41470176C>A Codon: GAG/TAG Consequence type: stop gained Cytogenetic band: 13q Genomic location: NC_000079.7:g.41470176C>A Locations: - p.Glu326Ter (Ensembl:ENSMUST00000163623) - c.976G>T (Ensembl:ENSMUST00000163623) Source type: large scale study Cross-references: | |||||||
rs3404075329 | 329 | T>P | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.3) Somatic: No Accession: NC_000079.7:g.41470167T>G Codon: ACA/CCA Consequence type: missense Cytogenetic band: 13q Genomic location: NC_000079.7:g.41470167T>G Locations: - p.Thr329Pro (Ensembl:ENSMUST00000163623) - c.985A>C (Ensembl:ENSMUST00000163623) Source type: large scale study Cross-references: | |||||||
rs3389287568 | 359 | D>E | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.26) Somatic: No Accession: NC_000079.7:g.41470075G>C Codon: GAC/GAG Consequence type: missense Cytogenetic band: 13q Genomic location: NC_000079.7:g.41470075G>C Locations: - p.Asp359Glu (Ensembl:ENSMUST00000163623) - c.1077C>G (Ensembl:ENSMUST00000163623) Source type: large scale study Cross-references: | |||||||
rs3389275401 | 360 | V>A | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.09) Somatic: No Accession: NC_000079.7:g.41470073A>G Codon: GTG/GCG Consequence type: missense Cytogenetic band: 13q Genomic location: NC_000079.7:g.41470073A>G Locations: - p.Val360Ala (Ensembl:ENSMUST00000163623) - c.1079T>C (Ensembl:ENSMUST00000163623) Source type: large scale study Cross-references: | |||||||
rs13470436 | 365 | N>S | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.01) Somatic: No Accession: NC_000079.7:g.41470058T>C Codon: AAC/AGC Consequence type: missense Cytogenetic band: 13q Genomic location: NC_000079.7:g.41470058T>C Locations: - p.Asn365Ser (Ensembl:ENSMUST00000163623) - c.1094A>G (Ensembl:ENSMUST00000163623) Source type: large scale study Cross-references: | |||||||
rs3389294586 | 365 | N>Y | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: NC_000079.7:g.41470059T>A Codon: AAC/TAC Consequence type: missense Cytogenetic band: 13q Genomic location: NC_000079.7:g.41470059T>A Locations: - p.Asn365Tyr (Ensembl:ENSMUST00000163623) - c.1093A>T (Ensembl:ENSMUST00000163623) Source type: large scale study Cross-references: | |||||||
rs3389253277 | 448 | R>S | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: NC_000079.7:g.41469810G>T Codon: CGC/AGC Consequence type: missense Cytogenetic band: 13q Genomic location: NC_000079.7:g.41469810G>T Locations: - p.Arg448Ser (Ensembl:ENSMUST00000163623) - c.1342C>A (Ensembl:ENSMUST00000163623) Source type: large scale study Cross-references: | |||||||
rs253382289 | 450 | A>S | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.1) Somatic: No Accession: NC_000079.7:g.41469804C>A Codon: GCG/TCG Consequence type: missense Cytogenetic band: 13q Genomic location: NC_000079.7:g.41469804C>A Locations: - p.Ala450Ser (Ensembl:ENSMUST00000163623) - c.1348G>T (Ensembl:ENSMUST00000163623) Source type: large scale study Cross-references: | |||||||
rs3389277335 | 451 | V>M | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.03) Somatic: No Accession: NC_000079.7:g.41469801C>T Codon: GTG/ATG Consequence type: missense Cytogenetic band: 13q Genomic location: NC_000079.7:g.41469801C>T Locations: - p.Val451Met (Ensembl:ENSMUST00000163623) - c.1351G>A (Ensembl:ENSMUST00000163623) Source type: large scale study Cross-references: | |||||||
rs3550098199 | 501 | T>P | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.09) Somatic: No Accession: NC_000079.7:g.41469651T>G Codon: ACC/CCC Consequence type: missense Cytogenetic band: 13q Genomic location: NC_000079.7:g.41469651T>G Locations: - p.Thr501Pro (Ensembl:ENSMUST00000163623) - c.1501A>C (Ensembl:ENSMUST00000163623) Source type: large scale study Cross-references: | |||||||
rs212296882 | 561 | A>G | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.85) Somatic: No Accession: NC_000079.7:g.41469470G>C Codon: GCC/GGC Consequence type: missense Cytogenetic band: 13q Genomic location: NC_000079.7:g.41469470G>C Locations: - p.Ala561Gly (Ensembl:ENSMUST00000163623) - c.1682C>G (Ensembl:ENSMUST00000163623) Source type: large scale study Cross-references: | |||||||
rs3389246352 | 577 | E>D | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (1) Somatic: No Accession: NC_000079.7:g.41469421C>A Codon: GAG/GAT Consequence type: missense Cytogenetic band: 13q Genomic location: NC_000079.7:g.41469421C>A Locations: - p.Glu577Asp (Ensembl:ENSMUST00000163623) - c.1731G>T (Ensembl:ENSMUST00000163623) Source type: large scale study Cross-references: | |||||||
rs3389208561 | 577 | E>K | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.12) Somatic: No Accession: NC_000079.7:g.41469423C>T Codon: GAG/AAG Consequence type: missense Cytogenetic band: 13q Genomic location: NC_000079.7:g.41469423C>T Locations: - p.Glu577Lys (Ensembl:ENSMUST00000163623) - c.1729G>A (Ensembl:ENSMUST00000163623) Source type: large scale study Cross-references: | |||||||
rs3389272988 | 579 | T>I | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.3) Somatic: No Accession: NC_000079.7:g.41469416G>A Codon: ACA/ATA Consequence type: missense Cytogenetic band: 13q Genomic location: NC_000079.7:g.41469416G>A Locations: - p.Thr579Ile (Ensembl:ENSMUST00000163623) - c.1736C>T (Ensembl:ENSMUST00000163623) Source type: large scale study Cross-references: | |||||||
rs3389294545 | 580 | H>Y | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.69) Somatic: No Accession: NC_000079.7:g.41469414G>A Codon: CAT/TAT Consequence type: missense Cytogenetic band: 13q Genomic location: NC_000079.7:g.41469414G>A Locations: - p.His580Tyr (Ensembl:ENSMUST00000163623) - c.1738C>T (Ensembl:ENSMUST00000163623) Source type: large scale study Cross-references: | |||||||
rs244535194 | 585 | M>V | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.41) Somatic: No Accession: NC_000079.7:g.41469399T>C Codon: ATG/GTG Consequence type: missense Cytogenetic band: 13q Genomic location: NC_000079.7:g.41469399T>C Locations: - p.Met585Val (Ensembl:ENSMUST00000163623) - c.1753A>G (Ensembl:ENSMUST00000163623) Source type: large scale study Cross-references: | |||||||
rs3404096972 | 587 | P>R | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.37) Somatic: No Accession: NC_000079.7:g.41469392G>C Codon: CCA/CGA Consequence type: missense Cytogenetic band: 13q Genomic location: NC_000079.7:g.41469392G>C Locations: - p.Pro587Arg (Ensembl:ENSMUST00000163623) - c.1760C>G (Ensembl:ENSMUST00000163623) Source type: large scale study Cross-references: | |||||||
rs3404092433 | 587 | P>S | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.57) Somatic: No Accession: NC_000079.7:g.41469393G>A Codon: CCA/TCA Consequence type: missense Cytogenetic band: 13q Genomic location: NC_000079.7:g.41469393G>A Locations: - p.Pro587Ser (Ensembl:ENSMUST00000163623) - c.1759C>T (Ensembl:ENSMUST00000163623) Source type: large scale study Cross-references: | |||||||
rs3389294570 | 607 | S>N | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.52) Somatic: No Accession: NC_000079.7:g.41469332C>T Codon: AGC/AAC Consequence type: missense Cytogenetic band: 13q Genomic location: NC_000079.7:g.41469332C>T Locations: - p.Ser607Asn (Ensembl:ENSMUST00000163623) - c.1820G>A (Ensembl:ENSMUST00000163623) Source type: large scale study Cross-references: | |||||||
rs3389281176 | 767 | A>T | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.84) Somatic: No Accession: NC_000079.7:g.41465340C>T Codon: GCT/ACT Consequence type: missense Cytogenetic band: 13q Genomic location: NC_000079.7:g.41465340C>T Locations: - p.Ala767Thr (Ensembl:ENSMUST00000163623) - c.2299G>A (Ensembl:ENSMUST00000163623) Source type: large scale study Cross-references: | |||||||
rs3404075338 | 791 | M>R | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.34) Somatic: No Accession: NC_000079.7:g.41465267A>C Codon: ATG/AGG Consequence type: missense Cytogenetic band: 13q Genomic location: NC_000079.7:g.41465267A>C Locations: - p.Met791Arg (Ensembl:ENSMUST00000163623) - c.2372T>G (Ensembl:ENSMUST00000163623) Source type: large scale study Cross-references: | |||||||
rs3403332636 | 793 | T>A | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: NC_000079.7:g.41465262T>C Codon: ACC/GCC Consequence type: missense Cytogenetic band: 13q Genomic location: NC_000079.7:g.41465262T>C Locations: - p.Thr793Ala (Ensembl:ENSMUST00000163623) - c.2377A>G (Ensembl:ENSMUST00000163623) Source type: large scale study Cross-references: |