WormBase Tree Display for Variation: WBVar01888364
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WBVar01888364 | Name | Public_name | WBVar01888364 | |||||
---|---|---|---|---|---|---|---|---|
Other_name | cewivar00603343 | |||||||
T06H11.1b.1:c.412-661G>A | ||||||||
T06H11.1a.1:c.526-661G>A | ||||||||
T06H11.1e.1:c.217-661G>A | ||||||||
T06H11.1d.1:c.442-661G>A | ||||||||
T06H11.1g.1:c.286-661G>A | ||||||||
T06H11.1f.1:c.562-661G>A | ||||||||
T06H11.1c.1:c.298-661G>A | ||||||||
HGVSg | CHROMOSOME_X:g.10108454C>T | |||||||
Sequence_details | SMap | S_parent | Sequence | T06H11 | ||||
Flanking_sequences | TTCAAACAAGATTTTGACTTTTCACTATAA | TCCTGTTCTATGTCACTCACAAAATAAGAT | ||||||
Mapping_target | T06H11 | |||||||
Source_location | 225 | CHROMOSOME_X | 10108395 | 10108395 | From_analysis | Million_mutation_project_reanalysis | ||
Type_of_mutation | Substitution | C | T | |||||
SeqStatus | Sequenced | |||||||
Variation_type | Natural_variant | |||||||
Origin | Species | Caenorhabditis elegans | ||||||
Strain | WBStrain00023072 | 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.412-661G>A | |||||||
Intron_number | 4/12 | |||||||
T06H11.1g.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | T06H11.1g.1:c.286-661G>A | |||||||
Intron_number | 3/12 | |||||||
T06H11.1f.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | T06H11.1f.1:c.562-661G>A | |||||||
Intron_number | 5/14 | |||||||
T06H11.1e.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | T06H11.1e.1:c.217-661G>A | |||||||
Intron_number | 3/13 | |||||||
T06H11.1d.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | T06H11.1d.1:c.442-661G>A | |||||||
Intron_number | 2/11 | |||||||
T06H11.1a.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | T06H11.1a.1:c.526-661G>A | |||||||
Intron_number | 2/11 | |||||||
T06H11.1c.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | T06H11.1c.1:c.298-661G>A | |||||||
Intron_number | 3/13 | |||||||
Method | WGS_Flibotte |