WormBase Tree Display for Variation: WBVar00466633
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| WBVar00466633 | Name | Public_name | gk243390 | ||
|---|---|---|---|---|---|
| Other_name (12) | |||||
| HGVSg | CHROMOSOME_V:g.9460075T>A | ||||
| Sequence_details | SMap | S_parent | Sequence | F07D3 | |
| Flanking_sequences | TTCACTTATTATAATTTTGAATTTCAGGTGGAAGACGATACTTCTCTGGC | ATGGAACAGAAAAAGATAGTTATGTGTGAAATTGACCGTTCAATTGAACG | |||
| Mapping_target | F07D3 | ||||
| Type_of_mutation | Substitution | T | A | ||
| SeqStatus | Sequenced | ||||
| Variation_type | Allele | ||||
| Origin | Species | Caenorhabditis elegans | |||
| Strain | WBStrain00038095 | ||||
| Laboratory | VC | ||||
| Analysis | Million_Mutation_Project | ||||
| Status | Live | ||||
| Affects | Gene | WBGene00019237 | |||
| Transcript | H24G06.1d.1 | VEP_consequence | synonymous_variant | ||
| VEP_impact | LOW | ||||
| HGVSc | H24G06.1d.1:c.1680T>A | ||||
| HGVSp | CE52360:p.Ala560= | ||||
| cDNA_position | 1680 | ||||
| CDS_position | 1680 | ||||
| Protein_position | 560 | ||||
| Exon_number | 8/9 | ||||
| Codon_change | gcT/gcA | ||||
| Amino_acid_change | A | ||||
| H24G06.1g.1 | VEP_consequence | synonymous_variant | |||
| VEP_impact | LOW | ||||
| HGVSc | H24G06.1g.1:c.1593T>A | ||||
| HGVSp | CE52263:p.Ala531= | ||||
| cDNA_position | 1593 | ||||
| CDS_position | 1593 | ||||
| Protein_position | 531 | ||||
| Exon_number | 7/8 | ||||
| Codon_change | gcT/gcA | ||||
| Amino_acid_change | A | ||||
| H24G06.1f.1 | VEP_consequence | synonymous_variant | |||
| VEP_impact | LOW | ||||
| HGVSc | H24G06.1f.1:c.1917T>A | ||||
| HGVSp | CE52347:p.Ala639= | ||||
| cDNA_position | 1917 | ||||
| CDS_position | 1917 | ||||
| Protein_position | 639 | ||||
| Exon_number | 9/10 | ||||
| Codon_change | gcT/gcA | ||||
| Amino_acid_change | A | ||||
| H24G06.1e.1 | VEP_consequence | synonymous_variant | |||
| VEP_impact | LOW | ||||
| HGVSc | H24G06.1e.1:c.1830T>A | ||||
| HGVSp | CE52098:p.Ala610= | ||||
| cDNA_position | 1830 | ||||
| CDS_position | 1830 | ||||
| Protein_position | 610 | ||||
| Exon_number | 8/9 | ||||
| Codon_change | gcT/gcA | ||||
| Amino_acid_change | A | ||||
| H24G06.1a.1 | VEP_consequence | synonymous_variant | |||
| VEP_impact | LOW | ||||
| HGVSc | H24G06.1a.1:c.4782T>A | ||||
| HGVSp | CE52314:p.Ala1594= | ||||
| cDNA_position | 4966 | ||||
| CDS_position | 4782 | ||||
| Protein_position | 1594 | ||||
| Exon_number | 25/27 | ||||
| Codon_change | gcT/gcA | ||||
| Amino_acid_change | A | ||||
| H24G06.1b.1 | VEP_consequence | synonymous_variant | |||
| VEP_impact | LOW | ||||
| HGVSc | H24G06.1b.1:c.4545T>A | ||||
| HGVSp | CE52223:p.Ala1515= | ||||
| cDNA_position | 4731 | ||||
| CDS_position | 4545 | ||||
| Protein_position | 1515 | ||||
| Exon_number | 24/26 | ||||
| Codon_change | gcT/gcA | ||||
| Amino_acid_change | A | ||||
| Reference | WBPaper00042537 | ||||
| Method | Million_mutation |
