A0A1Y7VM78 · A0A1Y7VM78_MOUSE
- Protein5-methyltetrahydrofolate-homocysteine methyltransferase reductase
- GeneMtrr
- StatusUniProtKB unreviewed (TrEMBL)
- Organism
- Amino acids
- Protein existenceEvidence at protein level
- Annotation score1/5
Variants
Variant ID(s) | Position(s) | Change | Description | Clinical significance | Provenance | ||
---|---|---|---|---|---|---|---|
rs3389298164 | 33 | A>V | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.04) Somatic: No Accession: NC_000079.7:g.68728701G>A Codon: GCA/GTA Consequence type: missense Cytogenetic band: 13q Genomic location: NC_000079.7:g.68728701G>A Locations: - p.Ala33Val (Ensembl:ENSMUST00000220973) - c.98C>T (Ensembl:ENSMUST00000220973) Source type: large scale study Cross-references: | |||||||
rs3389249625 | 35 | L>F | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: NC_000079.7:g.68728696G>A Codon: CTT/TTT Consequence type: missense Cytogenetic band: 13q Genomic location: NC_000079.7:g.68728696G>A Locations: - p.Leu35Phe (Ensembl:ENSMUST00000220973) - c.103C>T (Ensembl:ENSMUST00000220973) Source type: large scale study Cross-references: | |||||||
rs3389288339 | 39 | S>N | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.13) Somatic: No Accession: NC_000079.7:g.68728683C>T Codon: AGT/AAT Consequence type: missense Cytogenetic band: 13q Genomic location: NC_000079.7:g.68728683C>T Locations: - p.Ser39Asn (Ensembl:ENSMUST00000220973) - c.116G>A (Ensembl:ENSMUST00000220973) Source type: large scale study Cross-references: | |||||||
rs3389289029 | 43 | K>R | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.07) Somatic: No Accession: NC_000079.7:g.68728671T>C Codon: AAG/AGG Consequence type: missense Cytogenetic band: 13q Genomic location: NC_000079.7:g.68728671T>C Locations: - p.Lys43Arg (Ensembl:ENSMUST00000220973) - c.128A>G (Ensembl:ENSMUST00000220973) Source type: large scale study Cross-references: | |||||||
rs3389218436 | 49 | E>D | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0.01) Somatic: No Accession: NC_000079.7:g.68727798T>G Codon: GAA/GAC Consequence type: missense Cytogenetic band: 13q Genomic location: NC_000079.7:g.68727798T>G Locations: - p.Glu49Asp (Ensembl:ENSMUST00000220973) - c.147A>C (Ensembl:ENSMUST00000220973) Source type: large scale study Cross-references: | |||||||
rs3389275927 | 65 | P>S | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: NC_000079.7:g.68727752G>A Codon: CCA/TCA Consequence type: missense Cytogenetic band: 13q Genomic location: NC_000079.7:g.68727752G>A Locations: - p.Pro65Ser (Ensembl:ENSMUST00000220973) - c.193C>T (Ensembl:ENSMUST00000220973) Source type: large scale study Cross-references: | |||||||
rs51607956 | 90 | Q>R | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (1) Somatic: No Accession: NC_000079.7:g.68727676T>C Codon: CAA/CGA Consequence type: missense Cytogenetic band: 13q Genomic location: NC_000079.7:g.68727676T>C Locations: - p.Gln90Arg (Ensembl:ENSMUST00000220973) - c.269A>G (Ensembl:ENSMUST00000220973) Source type: large scale study Cross-references: |