A0AAA9S6R6 · A0AAA9S6R6_BOVIN
- ProteinProtein S100
- GeneS100A1
- StatusUniProtKB unreviewed (TrEMBL)
- Organism
- Amino acids139 (go to sequence)
- Protein existenceInferred from homology
- Annotation score2/5
Variants
Variant ID(s) | Position(s) | Change | Description | Clinical significance | Provenance | ||
---|---|---|---|---|---|---|---|
rs464543955 | 20 | C>F | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious - low confidence (0.01) Somatic: No Accession: NC_037330.1:g.16754199C>A Codon: TGT/TTT Consequence type: missense Cytogenetic band: Genomic location: NC_037330.1:g.16754199C>A Locations: - p.Cys20Phe (Ensembl:ENSBTAT00000126584) - c.59G>T (Ensembl:ENSBTAT00000126584) Source type: large scale study Cross-references: | |||||||
rs452543043 | 24 | T>P | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated - low confidence (0.12) Somatic: No Accession: NC_037330.1:g.16754188T>G Codon: ACC/CCC Consequence type: missense Cytogenetic band: Genomic location: NC_037330.1:g.16754188T>G Locations: - p.Thr24Pro (Ensembl:ENSBTAT00000126584) - c.70A>C (Ensembl:ENSBTAT00000126584) Source type: large scale study Cross-references: | |||||||
rs434036216 | 27 | G>A | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated - low confidence (0.93) Somatic: No Accession: NC_037330.1:g.16754178C>G Codon: GGC/GCC Consequence type: missense Cytogenetic band: Genomic location: NC_037330.1:g.16754178C>G Locations: - p.Gly27Ala (Ensembl:ENSBTAT00000126584) - c.80G>C (Ensembl:ENSBTAT00000126584) Source type: large scale study Cross-references: | |||||||
rs448242076 | 30 | T>P | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated - low confidence (0.31) Somatic: No Accession: NC_037330.1:g.16754170T>G Codon: ACA/CCA Consequence type: missense Cytogenetic band: Genomic location: NC_037330.1:g.16754170T>G Locations: - p.Thr30Pro (Ensembl:ENSBTAT00000126584) - c.88A>C (Ensembl:ENSBTAT00000126584) Source type: large scale study Cross-references: | |||||||
rs471257838 | 56 | T>P | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.02) Somatic: No Accession: NC_037330.1:g.16753397T>G Codon: ACT/CCT Consequence type: missense Cytogenetic band: Genomic location: NC_037330.1:g.16753397T>G Locations: - p.Thr56Pro (Ensembl:ENSBTAT00000126584) - c.166A>C (Ensembl:ENSBTAT00000126584) Source type: large scale study Cross-references: | |||||||
rs471257838 | 56 | T>S | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.46) Somatic: No Accession: NC_037330.1:g.16753397T>A Codon: ACT/TCT Consequence type: missense Cytogenetic band: Genomic location: NC_037330.1:g.16753397T>A Locations: - p.Thr56Ser (Ensembl:ENSBTAT00000126584) - c.166A>T (Ensembl:ENSBTAT00000126584) Source type: large scale study Cross-references: | |||||||
rs519826991 | 63 | A>T | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.66) Somatic: No Accession: NC_037330.1:g.16753376C>T Codon: GCC/ACC Consequence type: missense Cytogenetic band: Genomic location: NC_037330.1:g.16753376C>T Locations: - p.Ala63Thr (Ensembl:ENSBTAT00000126584) - c.187G>A (Ensembl:ENSBTAT00000126584) Source type: large scale study Cross-references: | |||||||
rs519264081 | 70 | D>Y | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: NC_037330.1:g.16753355C>A Codon: GAC/TAC Consequence type: missense Cytogenetic band: Genomic location: NC_037330.1:g.16753355C>A Locations: - p.Asp70Tyr (Ensembl:ENSBTAT00000126584) - c.208G>T (Ensembl:ENSBTAT00000126584) Source type: large scale study Cross-references: | |||||||
rs472324954 | 103 | V>G | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: NC_037330.1:g.16752080A>C Codon: GTG/GGG Consequence type: missense Cytogenetic band: Genomic location: NC_037330.1:g.16752080A>C Locations: - p.Val103Gly (Ensembl:ENSBTAT00000126584) - c.308T>G (Ensembl:ENSBTAT00000126584) Source type: large scale study Cross-references: | |||||||
rs799656897 | 111 | G>R | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.09) Somatic: No Accession: NC_037330.1:g.16752057C>G Codon: GGA/CGA Consequence type: missense Cytogenetic band: Genomic location: NC_037330.1:g.16752057C>G Locations: - p.Gly111Arg (Ensembl:ENSBTAT00000126584) - c.331G>C (Ensembl:ENSBTAT00000126584) Source type: large scale study Cross-references: | |||||||
rs453812824 | 115 | V>G | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.01) Somatic: No Accession: NC_037330.1:g.16752044A>C Codon: GTG/GGG Consequence type: missense Cytogenetic band: Genomic location: NC_037330.1:g.16752044A>C Locations: - p.Val115Gly (Ensembl:ENSBTAT00000126584) - c.344T>G (Ensembl:ENSBTAT00000126584) Source type: large scale study Cross-references: | |||||||
rs435005148 | 120 | Y>N | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: NC_037330.1:g.16752030A>T Codon: TAT/AAT Consequence type: missense Cytogenetic band: Genomic location: NC_037330.1:g.16752030A>T Locations: - p.Tyr120Asn (Ensembl:ENSBTAT00000126584) - c.358T>A (Ensembl:ENSBTAT00000126584) Source type: large scale study Cross-references: | |||||||
rs439645823 | 129 | V>E | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: NC_037330.1:g.16752002A>T Codon: GTG/GAG Consequence type: missense Cytogenetic band: Genomic location: NC_037330.1:g.16752002A>T Locations: - p.Val129Glu (Ensembl:ENSBTAT00000126584) - c.386T>A (Ensembl:ENSBTAT00000126584) Source type: large scale study Cross-references: | |||||||
rs467946735 | 135 | F>L | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.02) Somatic: No Accession: NC_037330.1:g.16751985A>G Codon: TTC/CTC Consequence type: missense Cytogenetic band: Genomic location: NC_037330.1:g.16751985A>G Locations: - p.Phe135Leu (Ensembl:ENSBTAT00000126584) - c.403T>C (Ensembl:ENSBTAT00000126584) Source type: large scale study Cross-references: |