Q61823 · PDCD4_MOUSE
- ProteinProgrammed cell death protein 4
- GenePdcd4
- StatusUniProtKB reviewed (Swiss-Prot)
- Organism
- Amino acids469 (go to sequence)
- Protein existenceEvidence at protein level
- Annotation score5/5
Variants
Variant ID(s) | Position(s) | Change | Description | Clinical significance | Provenance | ||
---|---|---|---|---|---|---|---|
rs3389546417 | 35 | E>K | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.68) Somatic: No Accession: NC_000085.7:g.53897602G>A Codon: GAA/AAA Consequence type: missense Cytogenetic band: 19q Genomic location: NC_000085.7:g.53897602G>A Locations: - p.Glu35Lys (Ensembl:ENSMUST00000074371) - c.103G>A (Ensembl:ENSMUST00000074371) - p.Glu35Lys (Ensembl:ENSMUST00000025931) - c.103G>A (Ensembl:ENSMUST00000025931) - p.Glu35Lys (Ensembl:ENSMUST00000165617) - c.103G>A (Ensembl:ENSMUST00000165617) Source type: large scale study Cross-references: | |||||||
rs3554407132 | 38 | N>K | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.3) Somatic: No Accession: NC_000085.7:g.53897613T>A Codon: AAT/AAA Consequence type: missense Cytogenetic band: 19q Genomic location: NC_000085.7:g.53897613T>A Locations: - p.Asn38Lys (Ensembl:ENSMUST00000074371) - c.114T>A (Ensembl:ENSMUST00000074371) - p.Asn38Lys (Ensembl:ENSMUST00000025931) - c.114T>A (Ensembl:ENSMUST00000025931) - p.Asn38Lys (Ensembl:ENSMUST00000165617) - c.114T>A (Ensembl:ENSMUST00000165617) Source type: large scale study Cross-references: | |||||||
rs3554514574 | 40 | I>R | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: NC_000085.7:g.53897618T>G Codon: ATA/AGA Consequence type: missense Cytogenetic band: 19q Genomic location: NC_000085.7:g.53897618T>G Locations: - p.Ile40Arg (Ensembl:ENSMUST00000074371) - c.119T>G (Ensembl:ENSMUST00000074371) - p.Ile40Arg (Ensembl:ENSMUST00000025931) - c.119T>G (Ensembl:ENSMUST00000025931) - p.Ile40Arg (Ensembl:ENSMUST00000165617) - c.119T>G (Ensembl:ENSMUST00000165617) Source type: large scale study Cross-references: | |||||||
rs3389555973 | 194 | G>E | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: NC_000085.7:g.53908071G>A Codon: GGG/GAG Consequence type: missense Cytogenetic band: 19q Genomic location: NC_000085.7:g.53908071G>A Locations: - p.Gly194Glu (Ensembl:ENSMUST00000074371) - c.581G>A (Ensembl:ENSMUST00000074371) - p.Gly194Glu (Ensembl:ENSMUST00000025931) - c.581G>A (Ensembl:ENSMUST00000025931) - p.Gly194Glu (Ensembl:ENSMUST00000165617) - c.581G>A (Ensembl:ENSMUST00000165617) Source type: large scale study Cross-references: | |||||||
rs3389513837 | 252 | L>M | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: NC_000085.7:g.53908244T>A Codon: TTG/ATG Consequence type: missense Cytogenetic band: 19q Genomic location: NC_000085.7:g.53908244T>A Locations: - p.Leu252Met (Ensembl:ENSMUST00000074371) - c.754T>A (Ensembl:ENSMUST00000074371) - p.Leu252Met (Ensembl:ENSMUST00000025931) - c.754T>A (Ensembl:ENSMUST00000025931) - p.Leu252Met (Ensembl:ENSMUST00000165617) - c.754T>A (Ensembl:ENSMUST00000165617) Source type: large scale study Cross-references: | |||||||
rs3389561488 | 289 | V>I | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.05) Somatic: No Accession: NC_000085.7:g.53909736G>A Codon: GTA/ATA Consequence type: missense Cytogenetic band: 19q Genomic location: NC_000085.7:g.53909736G>A Locations: - p.Val289Ile (Ensembl:ENSMUST00000074371) - c.865G>A (Ensembl:ENSMUST00000074371) - p.Val289Ile (Ensembl:ENSMUST00000025931) - c.865G>A (Ensembl:ENSMUST00000025931) - p.Val289Ile (Ensembl:ENSMUST00000165617) - c.865G>A (Ensembl:ENSMUST00000165617) Source type: large scale study Cross-references: | |||||||
rs3554364292 | 396 | I>V | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.43) Somatic: No Accession: NC_000085.7:g.53915053A>G Codon: ATT/GTT Consequence type: missense Cytogenetic band: 19q Genomic location: NC_000085.7:g.53915053A>G Locations: - p.Ile396Val (Ensembl:ENSMUST00000074371) - c.1186A>G (Ensembl:ENSMUST00000074371) - p.Ile396Val (Ensembl:ENSMUST00000025931) - c.1186A>G (Ensembl:ENSMUST00000025931) - p.Ile396Val (Ensembl:ENSMUST00000165617) - c.1186A>G (Ensembl:ENSMUST00000165617) Source type: large scale study Cross-references: | |||||||
rs3389494978 | 466 | P>T | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.57) Somatic: No Accession: NC_000085.7:g.53917560C>A Codon: CCT/ACT Consequence type: missense Cytogenetic band: 19q Genomic location: NC_000085.7:g.53917560C>A Locations: - p.Pro466Thr (Ensembl:ENSMUST00000074371) - c.1396C>A (Ensembl:ENSMUST00000074371) - p.Pro466Thr (Ensembl:ENSMUST00000025931) - c.1396C>A (Ensembl:ENSMUST00000025931) - p.Pro466Thr (Ensembl:ENSMUST00000165617) - c.1396C>A (Ensembl:ENSMUST00000165617) Source type: large scale study Cross-references: |