WormBase Tree Display for Variation: WBVar01826386
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WBVar01826386 | Name | Public_name | WBVar01826386 | |||||
---|---|---|---|---|---|---|---|---|
Other_name (11) | ||||||||
HGVSg | CHROMOSOME_I:g.4080128T>A | |||||||
Sequence_details | SMap | S_parent | Sequence | C24G7 | ||||
Flanking_sequences | CCAATAATTTTTTTTTAATTCTGGCGATGC | TCACCGTCGAGGTTCTCAAAACACAAAATC | ||||||
Mapping_target | C24G7 | |||||||
Source_location | 225 | CHROMOSOME_I | 4080130 | 4080130 | From_analysis | Million_mutation_project_reanalysis | ||
Type_of_mutation | Substitution | T | A | |||||
SeqStatus | Sequenced | |||||||
Variation_type | Natural_variant | |||||||
Origin | Species | Caenorhabditis elegans | ||||||
Strain | WBStrain00022886 | From_analysis | Million_mutation_project_reanalysis | |||||
Laboratory | VC | |||||||
Analysis | Million_mutation_project_reanalysis | |||||||
Status | Live | |||||||
Affects | Gene | WBGene00006820 | ||||||
Transcript | C09D1.1b.1 | VEP_consequence | intron_variant | |||||
VEP_impact | MODIFIER | |||||||
HGVSc | C09D1.1b.1:c.20087+412T>A | |||||||
Intron_number | 35/48 | |||||||
C09D1.1p.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | C09D1.1p.1:c.16508+412T>A | |||||||
Intron_number | 25/37 | |||||||
C09D1.1j.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | C09D1.1j.1:c.16748+412T>A | |||||||
Intron_number | 24/36 | |||||||
C09D1.1g.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | C09D1.1g.1:c.18668+412T>A | |||||||
Intron_number | 26/38 | |||||||
C09D1.1k.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | C09D1.1k.1:c.20021+412T>A | |||||||
Intron_number | 34/46 | |||||||
C09D1.1i.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | C09D1.1i.1:c.18602+412T>A | |||||||
Intron_number | 25/37 | |||||||
C09D1.1n.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | C09D1.1n.1:c.17927+412T>A | |||||||
Intron_number | 34/46 | |||||||
C09D1.1h.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | C09D1.1h.1:c.16949+412T>A | |||||||
Intron_number | 26/38 | |||||||
C09D1.1f.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | C09D1.1f.1:c.18167+412T>A | |||||||
Intron_number | 33/45 | |||||||
C09D1.1m.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | C09D1.1m.1:c.18368+412T>A | |||||||
Intron_number | 35/47 | |||||||
Method | WGS_Flibotte |