WormBase Tree Display for Variation: WBVar00144929
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| WBVar00144929 | Evidence | Paper_evidence (2) | |||||
|---|---|---|---|---|---|---|---|
| Name | Public_name | e2698 | |||||
| Other_name | CE28488:p.Ala131Val | ||||||
| T23F2.1b.1:c.434C>T | |||||||
| T23F2.1a.1:c.392C>T | |||||||
| CE54583:p.Ala145Val | |||||||
| HGVSg | CHROMOSOME_X:g.5494256C>T | ||||||
| Sequence_details | SMap | S_parent | Sequence | T23F2 | |||
| Flanking_sequences | cgtctcgatttttcctgtatagatggtatg | aaagctcatcggaatcgtcgaagaagaact | |||||
| Mapping_target | T23F2 | ||||||
| Type_of_mutation | Substitution | c | t | Paper_evidence | WBPaper00031667 | ||
| SeqStatus | Sequenced | ||||||
| Variation_type | Allele | ||||||
| Origin | Species | Caenorhabditis elegans | |||||
| Strain | WBStrain00004673 | ||||||
| WBStrain00047800 | |||||||
| Laboratory | CB | ||||||
| Status | Live | ||||||
| Affects | Gene | WBGene00044623 | |||||
| Transcript | T23F2.1b.1 | VEP_consequence | missense_variant | ||||
| VEP_impact | MODERATE | ||||||
| HGVSc | T23F2.1b.1:c.434C>T | ||||||
| HGVSp | CE54583:p.Ala145Val | ||||||
| cDNA_position | 434 | ||||||
| CDS_position | 434 | ||||||
| Protein_position | 145 | ||||||
| Exon_number | 4/9 | ||||||
| Codon_change | gCa/gTa | ||||||
| Amino_acid_change | A/V | ||||||
| T23F2.1a.1 (12) | |||||||
| Isolation | Mutagen | EMS | |||||
| Genetics | Interpolated_map_position | X | -5.24241 | ||||
| Description (2) | |||||||
| Reference | WBPaper00031667 | ||||||
| WBPaper00026735 | |||||||
| WBPaper00031925 | |||||||
| WBPaper00029153 | |||||||
| WBPaper00037686 | |||||||
| WBPaper00052991 | |||||||
| Method | Substitution_allele |
