WormBase Tree Display for Variation: WBVar01943146
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WBVar01943146 | Name | Public_name | WBVar01943146 | |||||
---|---|---|---|---|---|---|---|---|
Other_name | cewivar00664329 | |||||||
C09D1.1b.1:c.795+796_795+797insA | ||||||||
C09D1.1a.1:c.795+796_795+797insA | ||||||||
C09D1.1l.1:c.795+796_795+797insA | ||||||||
C09D1.1m.1:c.795+796_795+797insA | ||||||||
C09D1.1n.1:c.795+796_795+797insA | ||||||||
C09D1.1f.1:c.795+796_795+797insA | ||||||||
C09D1.1o.1:c.795+796_795+797insA | ||||||||
C09D1.1k.1:c.795+796_795+797insA | ||||||||
C09D1.1e.1:c.795+796_795+797insA | ||||||||
HGVSg | CHROMOSOME_I:g.4039668_4039669insA | |||||||
Sequence_details | SMap | S_parent | Sequence | C09D1 | ||||
Flanking_sequences | CGTAGAGATTTTATCTAATTACATATACTC | AAAAAAAAAACATAATAGTTTTTGACATAG | ||||||
Mapping_target | C09D1 | |||||||
Source_location | 225 | CHROMOSOME_I | 4039670 | 4039671 | From_analysis | Million_mutation_project_reanalysis | ||
Type_of_mutation | Insertion | A | ||||||
SeqStatus | Sequenced | |||||||
Variation_type | Natural_variant | |||||||
Origin | Species | Caenorhabditis elegans | ||||||
Strain | WBStrain00004599 | From_analysis | Million_mutation_project_reanalysis | |||||
WBStrain00027662 | From_analysis | Million_mutation_project_reanalysis | ||||||
Laboratory | VC | |||||||
Analysis | Million_mutation_project_reanalysis | |||||||
Status | Live | |||||||
Affects | Gene | WBGene00006820 | ||||||
Transcript | C09D1.1b.1 | VEP_consequence | intron_variant | |||||
VEP_impact | MODIFIER | |||||||
HGVSc | C09D1.1b.1:c.795+796_795+797insA | |||||||
Intron_number | 5/48 | |||||||
C09D1.1o.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | C09D1.1o.1:c.795+796_795+797insA | |||||||
Intron_number | 5/32 | |||||||
C09D1.1k.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | C09D1.1k.1:c.795+796_795+797insA | |||||||
Intron_number | 5/46 | |||||||
C09D1.1l.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | C09D1.1l.1:c.795+796_795+797insA | |||||||
Intron_number | 5/32 | |||||||
C09D1.1n.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | C09D1.1n.1:c.795+796_795+797insA | |||||||
Intron_number | 5/46 | |||||||
C09D1.1a.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | C09D1.1a.1:c.795+796_795+797insA | |||||||
Intron_number | 6/35 | |||||||
C09D1.1e.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | C09D1.1e.1:c.795+796_795+797insA | |||||||
Intron_number | 5/31 | |||||||
C09D1.1f.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | C09D1.1f.1:c.795+796_795+797insA | |||||||
Intron_number | 5/45 | |||||||
C09D1.1m.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | C09D1.1m.1:c.795+796_795+797insA | |||||||
Intron_number | 5/47 | |||||||
Method | WGS_Flibotte |