WormBase Tree Display for Variation: WBVar00090839
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WBVar00090839 | Evidence | Paper_evidence | WBPaper00031335 | ||
---|---|---|---|---|---|
Name | Public_name | n4438 | |||
Other_name | E01F3.1e.1:c.704+1618_705-2094del | ||||
E01F3.1h.1:c.392+1618_393-2094del | |||||
E01F3.1c.1:c.392+1618_393-2094del | |||||
E01F3.1i.1:c.704+1618_705-2094del | |||||
E01F3.1b.1:c.545+1618_546-2094del | |||||
E01F3.1f.1:c.404+1618_405-2094del | |||||
E01F3.1j.1:c.545+1618_546-2094del | |||||
E01F3.1g.1:c.404+1618_405-2094del | |||||
HGVSg | CHROMOSOME_II:g.14946935_14947697del | ||||
Sequence_details (5) | |||||
Variation_type | Allele | ||||
Origin | Species | Caenorhabditis elegans | |||
Strain | WBStrain00027453 | ||||
Laboratory | MT | ||||
Status | Live | ||||
Affects | Gene | WBGene00003366 | |||
WBGene00008443 | |||||
Transcript | E01F3.2 | ||||
E01F3.1f.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | E01F3.1f.1:c.404+1618_405-2094del | ||||
Intron_number | 3/10 | ||||
E01F3.1h.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | E01F3.1h.1:c.392+1618_393-2094del | ||||
Intron_number | 3/11 | ||||
E01F3.1j.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | E01F3.1j.1:c.545+1618_546-2094del | ||||
Intron_number | 4/11 | ||||
E01F3.1g.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | E01F3.1g.1:c.404+1618_405-2094del | ||||
Intron_number | 4/12 | ||||
E01F3.1i.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | E01F3.1i.1:c.704+1618_705-2094del | ||||
Intron_number | 5/12 | ||||
E01F3.1b.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | E01F3.1b.1:c.545+1618_546-2094del | ||||
Intron_number | 6/14 | ||||
E01F3.1c.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | E01F3.1c.1:c.392+1618_393-2094del | ||||
Intron_number | 3/11 | ||||
E01F3.1e.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | E01F3.1e.1:c.704+1618_705-2094del | ||||
Intron_number | 5/12 | ||||
Isolation | Mutagen | UV-TMP | Paper_evidence | WBPaper00031335 | |
Genetics | Interpolated_map_position | II | 23.7727 | ||
Description | Phenotype_not_observed (9) | ||||
Reference | WBPaper00031335 | ||||
WBPaper00035558 | |||||
Method | Deletion_allele |