B6VQA5 · SPT31_RAT
- ProteinSpermatogenesis-associated protein 31
- GeneSpata31
- StatusUniProtKB reviewed (Swiss-Prot)
- Organism
- Amino acids1048 (go to sequence)
- Protein existenceEvidence at protein level
- Annotation score4/5
Variants
Variant ID(s) | Position(s) | Change | Description | Clinical significance | Provenance | ||
---|---|---|---|---|---|---|---|
rs196981751 | 233 | P>R | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.89) Somatic: No Accession: NC_051352.1:g.246196G>C Codon: CCA/CGA Consequence type: missense Cytogenetic band: 17chr Genomic location: NC_051352.1:g.246196G>C Locations: - p.Pro233Arg (Ensembl:ENSRNOT00000024504) - c.698C>G (Ensembl:ENSRNOT00000024504) Source type: large scale study Cross-references: | |||||||
rs3322931924 | 313 | D>E | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (1) Somatic: No Accession: NC_051352.1:g.245955A>T Codon: GAT/GAA Consequence type: missense Cytogenetic band: 17chr Genomic location: NC_051352.1:g.245955A>T Locations: - p.Asp313Glu (Ensembl:ENSRNOT00000024504) - c.939T>A (Ensembl:ENSRNOT00000024504) Source type: large scale study Cross-references: | |||||||
rs199076562 | 451 | N>K | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.04) Somatic: No Accession: NC_051352.1:g.245541A>C Codon: AAT/AAG Consequence type: missense Cytogenetic band: 17chr Genomic location: NC_051352.1:g.245541A>C Locations: - p.Asn451Lys (Ensembl:ENSRNOT00000024504) - c.1353T>G (Ensembl:ENSRNOT00000024504) Source type: large scale study Cross-references: | |||||||
rs197217439 | 451 | N>T | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.03) Somatic: No Accession: NC_051352.1:g.245542T>G Codon: AAT/ACT Consequence type: missense Cytogenetic band: 17chr Genomic location: NC_051352.1:g.245542T>G Locations: - p.Asn451Thr (Ensembl:ENSRNOT00000024504) - c.1352A>C (Ensembl:ENSRNOT00000024504) Source type: large scale study Cross-references: | |||||||
rs198408700 | 746 | P>S | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.24) Somatic: No Accession: NC_051352.1:g.244658G>A Codon: CCT/TCT Consequence type: missense Cytogenetic band: 17chr Genomic location: NC_051352.1:g.244658G>A Locations: - p.Pro746Ser (Ensembl:ENSRNOT00000024504) - c.2236C>T (Ensembl:ENSRNOT00000024504) Source type: large scale study Cross-references: | |||||||
rs3323074684 | 817 | T>M | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.03) Somatic: No Accession: NC_051352.1:g.244444G>A Codon: ACG/ATG Consequence type: missense Cytogenetic band: 17chr Genomic location: NC_051352.1:g.244444G>A Locations: - p.Thr817Met (Ensembl:ENSRNOT00000024504) - c.2450C>T (Ensembl:ENSRNOT00000024504) Source type: large scale study Cross-references: |