WormBase Tree Display for Variation: WBVar01681600
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WBVar01681600 | Name | Public_name | WBVar01681600 | |||||
---|---|---|---|---|---|---|---|---|
Other_name | cewivar00372147 | |||||||
Y43H11AL.1c.1:c.494+137T>A | ||||||||
Y43H11AL.1b.1:c.536+137T>A | ||||||||
Y43H11AL.1a.4:c.536+137T>A | ||||||||
Y43H11AL.1a.3:c.536+137T>A | ||||||||
Y43H11AL.1a.1:c.536+137T>A | ||||||||
Y43H11AL.1a.2:c.536+137T>A | ||||||||
HGVSg | CHROMOSOME_II:g.230730A>T | |||||||
Sequence_details | SMap | S_parent | Sequence | Y43H11AL | ||||
Flanking_sequences | TTTCAGATTTCTCCGATTTTTTTAAAAATC | TTTTTTTTAATCTAAAAATTTATATATTTT | ||||||
Mapping_target | Y43H11AL | |||||||
Source_location | 225 | CHROMOSOME_II | 230730 | 230730 | From_analysis | Million_mutation_project_reanalysis | ||
Type_of_mutation | Substitution | A | T | |||||
SeqStatus | Sequenced | |||||||
Variation_type | Natural_variant | |||||||
Origin | Species | Caenorhabditis elegans | ||||||
Strain | WBStrain00006640 | From_analysis | Million_mutation_project_reanalysis | |||||
WBStrain00023138 | From_analysis | Million_mutation_project_reanalysis | ||||||
Laboratory | VC | |||||||
Analysis | Million_mutation_project_reanalysis | |||||||
Status | Live | |||||||
Affects | Gene | WBGene00021545 | ||||||
Transcript | Y43H11AL.1a.3 | VEP_consequence | intron_variant | |||||
VEP_impact | MODIFIER | |||||||
HGVSc | Y43H11AL.1a.3:c.536+137T>A | |||||||
Intron_number | 4/10 | |||||||
Y43H11AL.1c.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | Y43H11AL.1c.1:c.494+137T>A | |||||||
Intron_number | 2/8 | |||||||
Y43H11AL.1b.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | Y43H11AL.1b.1:c.536+137T>A | |||||||
Intron_number | 4/11 | |||||||
Y43H11AL.1a.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | Y43H11AL.1a.1:c.536+137T>A | |||||||
Intron_number | 4/10 | |||||||
Y43H11AL.1a.2 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | Y43H11AL.1a.2:c.536+137T>A | |||||||
Intron_number | 4/8 | |||||||
Y43H11AL.1a.4 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | Y43H11AL.1a.4:c.536+137T>A | |||||||
Intron_number | 4/9 | |||||||
Method | WGS_Flibotte |