A0A140LI24 · A0A140LI24_MOUSE
- ProteinAvian reticuloendotheliosis viral (v-rel) oncogene related B
- GeneRelb
- StatusUniProtKB unreviewed (TrEMBL)
- Organism
- Amino acids116 (go to sequence)
- Protein existenceEvidence at protein level
- Annotation score1/5
Variants
Variant ID(s) | Position(s) | Change | Description | Clinical significance | Provenance | ||
---|---|---|---|---|---|---|---|
rs3388860178 | 20 | A>V | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.45) Somatic: No Accession: NC_000073.7:g.19353647G>A Codon: GCT/GTT Consequence type: missense Cytogenetic band: 7q Genomic location: NC_000073.7:g.19353647G>A Locations: - p.Ala20Val (Ensembl:ENSMUST00000141586) - c.59C>T (Ensembl:ENSMUST00000141586) Source type: large scale study Cross-references: | |||||||
rs3388865119 | 27 | T>M | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.1) Somatic: No Accession: NC_000073.7:g.19353626G>A Codon: ACG/ATG Consequence type: missense Cytogenetic band: 7q Genomic location: NC_000073.7:g.19353626G>A Locations: - p.Thr27Met (Ensembl:ENSMUST00000141586) - c.80C>T (Ensembl:ENSMUST00000141586) Source type: large scale study Cross-references: | |||||||
rs3388891639 | 30 | W>* | EVA | ||||
Consequence: stop gained Somatic: No Accession: NC_000073.7:g.19353616C>T Codon: TGG/TGA Consequence type: stop gained Cytogenetic band: 7q Genomic location: NC_000073.7:g.19353616C>T Locations: - p.Trp30Ter (Ensembl:ENSMUST00000141586) - c.90G>A (Ensembl:ENSMUST00000141586) Source type: large scale study Cross-references: | |||||||
rs3388877103 | 56 | Q>L | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: NC_000073.7:g.19353539T>A Codon: CAG/CTG Consequence type: missense Cytogenetic band: 7q Genomic location: NC_000073.7:g.19353539T>A Locations: - p.Gln56Leu (Ensembl:ENSMUST00000141586) - c.167A>T (Ensembl:ENSMUST00000141586) Source type: large scale study Cross-references: | |||||||
rs3397263110 | 64-65 | EC>RP | EVA | ||||
Consequence: stop gained Somatic: No Accession: NC_000073.7:g.19353517_19353518insCAGCGTGGCATGCGCTTCCGCTACGAGTGCGAGGGCCGCTCG Codon: -/CGGCCCTCGCACTCGTAGCGGAAGCGCATGCCACGCTGCGAG Consequence type: stop gained Cytogenetic band: 7q Genomic location: NC_000073.7:g.19353517_19353518insCAGCGTGGCATGCGCTTCCGCTACGAGTGCGAGGGCCGCTCG Locations: - p.Glu64_Cys65insArgProSerHisSerTer (Ensembl:ENSMUST00000141586) - c.192_193insCGGCCCTCGCACTCGTAGCGGAAGCGCATGCCACGCTGCGAG (Ensembl:ENSMUST00000141586) Source type: large scale study Cross-references: | |||||||
rs3388885577 | 94 | G>V | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.06) Somatic: No Accession: NC_000073.7:g.19351831C>A Codon: GGC/GTC Consequence type: missense Cytogenetic band: 7q Genomic location: NC_000073.7:g.19351831C>A Locations: - p.Gly94Val (Ensembl:ENSMUST00000141586) - c.281G>T (Ensembl:ENSMUST00000141586) Source type: large scale study Cross-references: | |||||||
rs3412969166 | 105 | L>P | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: NC_000073.7:g.19351798A>G Codon: CTG/CCG Consequence type: missense Cytogenetic band: 7q Genomic location: NC_000073.7:g.19351798A>G Locations: - p.Leu105Pro (Ensembl:ENSMUST00000141586) - c.314T>C (Ensembl:ENSMUST00000141586) Source type: large scale study Cross-references: | |||||||
rs3397420581 | 108 | K>M | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: NC_000073.7:g.19351789T>A Codon: AAG/ATG Consequence type: missense Cytogenetic band: 7q Genomic location: NC_000073.7:g.19351789T>A Locations: - p.Lys108Met (Ensembl:ENSMUST00000141586) - c.323A>T (Ensembl:ENSMUST00000141586) Source type: large scale study Cross-references: | |||||||
rs3397728888 | 109 | D>A | EVA | ||||
Consequence: missense Predictions: - SIFT: deleterious (0) Somatic: No Accession: NC_000073.7:g.19351786T>G Codon: GAC/GCC Consequence type: missense Cytogenetic band: 7q Genomic location: NC_000073.7:g.19351786T>G Locations: - p.Asp109Ala (Ensembl:ENSMUST00000141586) - c.326A>C (Ensembl:ENSMUST00000141586) Source type: large scale study Cross-references: | |||||||
rs3397728909 | 110 | W>L | EVA | ||||
Consequence: missense Predictions: - SIFT: tolerated (0.75) Somatic: No Accession: NC_000073.7:g.19351783C>A Codon: TGG/TTG Consequence type: missense Cytogenetic band: 7q Genomic location: NC_000073.7:g.19351783C>A Locations: - p.Trp110Leu (Ensembl:ENSMUST00000141586) - c.329G>T (Ensembl:ENSMUST00000141586) Source type: large scale study Cross-references: |