A0A140LHC9 · A0A140LHC9_MOUSE
- ProteinSolute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6
- GeneSlc17a6
- StatusUniProtKB unreviewed (TrEMBL)
- Organism
- Amino acids202 (go to sequence)
- Protein existenceEvidence at protein level
- Annotation score1/5
Variants
Variant ID(s) | Position(s) | Change | Description | Clinical significance | Provenance | ||
---|---|---|---|---|---|---|---|
rs3388892689 | 11 | P>S | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated - low confidence (0.09) Somatic: No Accession: NC_000073.7:g.51272413C>T Codon: CCG/TCG Consequence type: missense Cytogenetic band: 7q Genomic location: NC_000073.7:g.51272413C>T Locations: - p.Pro11Ser (Ensembl:ENSMUST00000207945) - c.31C>T (Ensembl:ENSMUST00000207945) Source type: large scale study Cross-references: | |||||||
rs3388913769 | 30 | V>M | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious - low confidence (0.03) Somatic: No Accession: NC_000073.7:g.51275030G>A Codon: GTG/ATG Consequence type: missense Cytogenetic band: 7q Genomic location: NC_000073.7:g.51275030G>A Locations: - p.Val30Met (Ensembl:ENSMUST00000207945) - c.88G>A (Ensembl:ENSMUST00000207945) Source type: large scale study Cross-references: | |||||||
rs3388905920 | 57 | A>T | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated - low confidence (0.19) Somatic: No Accession: NC_000073.7:g.51275111G>A Codon: GCT/ACT Consequence type: missense Cytogenetic band: 7q Genomic location: NC_000073.7:g.51275111G>A Locations: - p.Ala57Thr (Ensembl:ENSMUST00000207945) - c.169G>A (Ensembl:ENSMUST00000207945) Source type: large scale study Cross-references: | |||||||
rs3388887659 | 81 | F>S | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious - low confidence (0) Somatic: No Accession: NC_000073.7:g.51275184T>C Codon: TTC/TCC Consequence type: missense Cytogenetic band: 7q Genomic location: NC_000073.7:g.51275184T>C Locations: - p.Phe81Ser (Ensembl:ENSMUST00000207945) - c.242T>C (Ensembl:ENSMUST00000207945) Source type: large scale study Cross-references: | |||||||
rs3388916907 | 85 | F>L | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious - low confidence (0) Somatic: No Accession: NC_000073.7:g.51275197C>A Codon: TTC/TTA Consequence type: missense Cytogenetic band: 7q Genomic location: NC_000073.7:g.51275197C>A Locations: - p.Phe85Leu (Ensembl:ENSMUST00000207945) - c.255C>A (Ensembl:ENSMUST00000207945) Source type: large scale study Cross-references: | |||||||
rs3388912610 | 121 | P>L | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious - low confidence (0) Somatic: No Accession: NC_000073.7:g.51276614C>T Codon: CCC/CTC Consequence type: missense Cytogenetic band: 7q Genomic location: NC_000073.7:g.51276614C>T Locations: - p.Pro121Leu (Ensembl:ENSMUST00000207945) - c.362C>T (Ensembl:ENSMUST00000207945) Source type: large scale study Cross-references: | |||||||
rs3388887695 | 126 | M>V | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious - low confidence (0) Somatic: No Accession: NC_000073.7:g.51276628A>G Codon: ATG/GTG Consequence type: missense Cytogenetic band: 7q Genomic location: NC_000073.7:g.51276628A>G Locations: - p.Met126Val (Ensembl:ENSMUST00000207945) - c.376A>G (Ensembl:ENSMUST00000207945) Source type: large scale study Cross-references: | |||||||
rs3388910495 | 139 | Q>E | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious - low confidence (0) Somatic: No Accession: NC_000073.7:g.51276667C>G Codon: CAG/GAG Consequence type: missense Cytogenetic band: 7q Genomic location: NC_000073.7:g.51276667C>G Locations: - p.Gln139Glu (Ensembl:ENSMUST00000207945) - c.415C>G (Ensembl:ENSMUST00000207945) Source type: large scale study Cross-references: | |||||||
rs3388896564 | 185 | I>K | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious - low confidence (0) Somatic: No Accession: NC_000073.7:g.51294848T>A Codon: ATA/AAA Consequence type: missense Cytogenetic band: 7q Genomic location: NC_000073.7:g.51294848T>A Locations: - p.Ile185Lys (Ensembl:ENSMUST00000207945) - c.554T>A (Ensembl:ENSMUST00000207945) Source type: large scale study Cross-references: | |||||||
rs237776647 | 199 | L>S | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious - low confidence (0.01) Somatic: No Accession: NC_000073.7:g.51298922T>C Codon: TTG/TCG Consequence type: missense Cytogenetic band: 7q Genomic location: NC_000073.7:g.51298922T>C Locations: - p.Leu199Ser (Ensembl:ENSMUST00000207945) - c.596T>C (Ensembl:ENSMUST00000207945) Source type: large scale study Cross-references: |