WormBase Tree Display for Variation: WBVar01902373
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WBVar01902373 | Name | Public_name | WBVar01902373 | |||||
---|---|---|---|---|---|---|---|---|
Other_name | cewivar00617958 | |||||||
B0041.2a.2:c.1418-119C>T | ||||||||
B0041.2g.1:c.1358-119C>T | ||||||||
B0041.2c.1:c.1412-119C>T | ||||||||
B0041.2e.1:c.1484-119C>T | ||||||||
B0041.2d.1:c.1544-119C>T | ||||||||
B0041.2a.1:c.1418-119C>T | ||||||||
B0041.2b.1:c.1538-119C>T | ||||||||
B0041.2f.1:c.1478-119C>T | ||||||||
HGVSg | CHROMOSOME_I:g.4657820C>T | |||||||
Sequence_details | SMap | S_parent | Sequence | B0041 | ||||
Flanking_sequences | CTGTAAAATCGCGCGTAGTCCACCGGAAAT | GACATGAGATCTCATGTCGATTTACAGTGG | ||||||
Mapping_target | B0041 | |||||||
Source_location | 225 | CHROMOSOME_I | 4657821 | 4657821 | From_analysis | Million_mutation_project_reanalysis | ||
Type_of_mutation | Substitution | C | T | |||||
SeqStatus | Sequenced | |||||||
Variation_type | Natural_variant | |||||||
Origin | Species | Caenorhabditis elegans | ||||||
Strain | WBStrain00027647 | From_analysis | Million_mutation_project_reanalysis | |||||
Laboratory | VC | |||||||
Analysis | Million_mutation_project_reanalysis | |||||||
Status | Live | |||||||
Affects | Gene | WBGene00015007 | ||||||
Transcript | B0041.2f.1 | VEP_consequence | intron_variant | |||||
VEP_impact | MODIFIER | |||||||
HGVSc | B0041.2f.1:c.1478-119C>T | |||||||
Intron_number | 7/10 | |||||||
B0041.2d.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | B0041.2d.1:c.1544-119C>T | |||||||
Intron_number | 6/8 | |||||||
B0041.2c.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | B0041.2c.1:c.1412-119C>T | |||||||
Intron_number | 5/8 | |||||||
B0041.2e.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | B0041.2e.1:c.1484-119C>T | |||||||
Intron_number | 7/10 | |||||||
B0041.2a.2 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | B0041.2a.2:c.1418-119C>T | |||||||
Intron_number | 5/8 | |||||||
B0041.2a.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | B0041.2a.1:c.1418-119C>T | |||||||
Intron_number | 7/10 | |||||||
B0041.2g.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | B0041.2g.1:c.1358-119C>T | |||||||
Intron_number | 5/8 | |||||||
B0041.2b.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | B0041.2b.1:c.1538-119C>T | |||||||
Intron_number | 7/10 | |||||||
Method | WGS_Flibotte |