WormBase Tree Display for Variation: WBVar01551603
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WBVar01551603 | Name | Public_name | WBVar01551603 | |||||
---|---|---|---|---|---|---|---|---|
Other_name | cewivar00128660 | |||||||
T06H11.1g.1:c.136+1886G>T | ||||||||
T06H11.1f.1:c.413-2455G>T | ||||||||
T06H11.1d.1:c.293-2455G>T | ||||||||
T06H11.1b.1:c.263-2455G>T | ||||||||
T06H11.1c.1:c.149-2455G>T | ||||||||
HGVSg | CHROMOSOME_X:g.10111786C>A | |||||||
Sequence_details | SMap | S_parent | Sequence | T06H11 | ||||
Flanking_sequences | CTAATTCAAACTTTTTTGTTTTTTCTGCTG | AAAATTCAAATTACTTTGTAGATTGGTTTT | ||||||
Mapping_target | T06H11 | |||||||
Source_location | 225 | CHROMOSOME_X | 10111727 | 10111727 | From_analysis | Million_mutation_project_reanalysis | ||
Type_of_mutation | Substitution | C | A | |||||
SeqStatus | Sequenced | |||||||
Variation_type | Natural_variant | |||||||
Origin | Species | Caenorhabditis elegans | ||||||
Strain | WBStrain00004599 | From_analysis | Million_mutation_project_reanalysis | |||||
WBStrain00022850 | From_analysis | Million_mutation_project_reanalysis | ||||||
WBStrain00023139 | From_analysis | Million_mutation_project_reanalysis | ||||||
WBStrain00023192 | From_analysis | Million_mutation_project_reanalysis | ||||||
WBStrain00024204 | From_analysis | Million_mutation_project_reanalysis | ||||||
WBStrain00027647 | From_analysis | Million_mutation_project_reanalysis | ||||||
WBStrain00027648 | From_analysis | Million_mutation_project_reanalysis | ||||||
WBStrain00027660 | From_analysis | Million_mutation_project_reanalysis | ||||||
Laboratory | VC | |||||||
Analysis | Million_mutation_project_reanalysis | |||||||
Status | Live | |||||||
Affects | Gene | WBGene00006792 | ||||||
Transcript | T06H11.1b.1 | VEP_consequence | intron_variant | |||||
VEP_impact | MODIFIER | |||||||
HGVSc | T06H11.1b.1:c.263-2455G>T | |||||||
Intron_number | 3/12 | |||||||
T06H11.1g.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | T06H11.1g.1:c.136+1886G>T | |||||||
Intron_number | 2/12 | |||||||
T06H11.1f.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | T06H11.1f.1:c.413-2455G>T | |||||||
Intron_number | 4/14 | |||||||
T06H11.1d.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | T06H11.1d.1:c.293-2455G>T | |||||||
Intron_number | 1/11 | |||||||
T06H11.1c.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | T06H11.1c.1:c.149-2455G>T | |||||||
Intron_number | 2/13 | |||||||
Method | WGS_Flibotte |