WormBase Tree Display for Variation: WBVar01786909
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WBVar01786909 | Name | Public_name | WBVar01786909 | |||||
---|---|---|---|---|---|---|---|---|
Other_name | cewivar00488800 | |||||||
T06H11.1d.1:c.293-3765T>C | ||||||||
T06H11.1b.1:c.263-3765T>C | ||||||||
T06H11.1g.1:c.136+576T>C | ||||||||
T06H11.1f.1:c.413-3765T>C | ||||||||
T06H11.1c.1:c.149-3765T>C | ||||||||
HGVSg | CHROMOSOME_X:g.10113096A>G | |||||||
Sequence_details | SMap | S_parent | Sequence | T06H11 | ||||
Flanking_sequences | GGTATCTAATACTGCTCAGTTCTGAATTTA | TTTTTGATATGTATTCAACTAATGGTCTAA | ||||||
Mapping_target | T06H11 | |||||||
Source_location | 225 | CHROMOSOME_X | 10113037 | 10113037 | From_analysis | Million_mutation_project_reanalysis | ||
Type_of_mutation | Substitution | A | G | |||||
SeqStatus | Sequenced | |||||||
Variation_type | Natural_variant | |||||||
Origin | Species | Caenorhabditis elegans | ||||||
Strain | WBStrain00022850 | 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 | ||||||
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.263-3765T>C | |||||||
Intron_number | 3/12 | |||||||
T06H11.1g.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | T06H11.1g.1:c.136+576T>C | |||||||
Intron_number | 2/12 | |||||||
T06H11.1f.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | T06H11.1f.1:c.413-3765T>C | |||||||
Intron_number | 4/14 | |||||||
T06H11.1d.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | T06H11.1d.1:c.293-3765T>C | |||||||
Intron_number | 1/11 | |||||||
T06H11.1c.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | T06H11.1c.1:c.149-3765T>C | |||||||
Intron_number | 2/13 | |||||||
Method | WGS_Flibotte |