WormBase Tree Display for Variation: WBVar02012643
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WBVar02012643 | Name | Public_name | WBVar02012643 | |||||
---|---|---|---|---|---|---|---|---|
Other_name | cewivar00741060 | |||||||
F42G9.6b.1:c.*251dup | ||||||||
F42G9.6c.1:c.*251dup | ||||||||
F42G9.6a.1:c.*251dup | ||||||||
F42G9.5b.2:c.-7+384dup | ||||||||
HGVSg | CHROMOSOME_III:g.778430_778431insA | |||||||
Sequence_details | SMap | S_parent | Sequence | F42G9 | ||||
Flanking_sequences | AAACCTTCGAAAACAAATGGCTTTAAAAAC | AAAAATGGGGTTTTGGAAAATGTGGATTTT | ||||||
Mapping_target | F42G9 | |||||||
Source_location | 225 | CHROMOSOME_III | 778426 | 778427 | From_analysis | Million_mutation_project_reanalysis | ||
Type_of_mutation | Insertion | A | ||||||
SeqStatus | Sequenced | |||||||
Variation_type | Natural_variant | |||||||
Origin | Species | Caenorhabditis elegans | ||||||
Strain | WBStrain00008273 | From_analysis | Million_mutation_project_reanalysis | |||||
WBStrain00022850 | From_analysis | Million_mutation_project_reanalysis | ||||||
WBStrain00023138 | From_analysis | Million_mutation_project_reanalysis | ||||||
WBStrain00023191 | From_analysis | Million_mutation_project_reanalysis | ||||||
WBStrain00027647 | From_analysis | Million_mutation_project_reanalysis | ||||||
WBStrain00031113 | From_analysis | Million_mutation_project_reanalysis | ||||||
Laboratory | VC | |||||||
Analysis | Million_mutation_project_reanalysis | |||||||
Status | Live | |||||||
Affects | Gene | WBGene00018364 | ||||||
WBGene00000117 | ||||||||
Transcript | F42G9.6c.1 | VEP_consequence | 3_prime_UTR_variant | |||||
VEP_impact | MODIFIER | |||||||
HGVSc | F42G9.6c.1:c.*251dup | |||||||
cDNA_position | 2241-2242 | |||||||
Exon_number | 11/11 | |||||||
F42G9.6a.1 | VEP_consequence | 3_prime_UTR_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F42G9.6a.1:c.*251dup | |||||||
cDNA_position | 2233-2234 | |||||||
Exon_number | 11/11 | |||||||
F42G9.5b.2 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F42G9.5b.2:c.-7+384dup | |||||||
Intron_number | 1/7 | |||||||
F42G9.6b.1 | VEP_consequence | 3_prime_UTR_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F42G9.6b.1:c.*251dup | |||||||
cDNA_position | 2313-2314 | |||||||
Exon_number | 12/12 | |||||||
Method | WGS_Flibotte |