WormBase Tree Display for Variation: WBVar02068660
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WBVar02068660 | Name | Public_name | WBVar02068660 | |||||
---|---|---|---|---|---|---|---|---|
Other_name | cewivar00797927 | |||||||
F18F11.3b.1:c.342+83_342+84insT | ||||||||
F18F11.3f.1:c.342+83_342+84insT | ||||||||
F18F11.3e.1:c.342+83_342+84insT | ||||||||
F18F11.3d.1:c.342+83_342+84insT | ||||||||
F18F11.3a.1:c.342+83_342+84insT | ||||||||
F18F11.3h.1:c.342+83_342+84insT | ||||||||
F18F11.3c.1:c.342+83_342+84insT | ||||||||
F18F11.3g.1:c.342+83_342+84insT | ||||||||
HGVSg | CHROMOSOME_IV:g.345342_345343insT | |||||||
Sequence_details | SMap | S_parent | Sequence | F18F11 | ||||
Flanking_sequences | AAATTTAGTGGTTCAACATGTTTTTTCGTG | TTTTTTTTTTGTTTTTGCAGAGAAAACCGA | ||||||
Mapping_target | F18F11 | |||||||
Source_location | 225 | CHROMOSOME_IV | 345342 | 345343 | From_analysis | Million_mutation_project_reanalysis | ||
Type_of_mutation | Insertion | T | ||||||
SeqStatus | Sequenced | |||||||
Variation_type | Natural_variant | |||||||
Origin | Species | Caenorhabditis elegans | ||||||
Strain | WBStrain00024204 | From_analysis | Million_mutation_project_reanalysis | |||||
Laboratory | VC | |||||||
Analysis | Million_mutation_project_reanalysis | |||||||
Status | Live | |||||||
Affects | Gene | WBGene00017576 | ||||||
Transcript | F18F11.3e.1 | VEP_consequence | intron_variant | |||||
VEP_impact | MODIFIER | |||||||
HGVSc | F18F11.3e.1:c.342+83_342+84insT | |||||||
Intron_number | 4/25 | |||||||
F18F11.3g.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F18F11.3g.1:c.342+83_342+84insT | |||||||
Intron_number | 4/25 | |||||||
F18F11.3f.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F18F11.3f.1:c.342+83_342+84insT | |||||||
Intron_number | 4/24 | |||||||
F18F11.3h.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F18F11.3h.1:c.342+83_342+84insT | |||||||
Intron_number | 4/26 | |||||||
F18F11.3d.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F18F11.3d.1:c.342+83_342+84insT | |||||||
Intron_number | 4/25 | |||||||
F18F11.3a.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F18F11.3a.1:c.342+83_342+84insT | |||||||
Intron_number | 4/25 | |||||||
F18F11.3b.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F18F11.3b.1:c.342+83_342+84insT | |||||||
Intron_number | 4/23 | |||||||
F18F11.3c.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F18F11.3c.1:c.342+83_342+84insT | |||||||
Intron_number | 4/24 | |||||||
Method | WGS_Flibotte |