WormBase Tree Display for Variation: WBVar01607160
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WBVar01607160 | Name | Public_name | WBVar01607160 | |||||
---|---|---|---|---|---|---|---|---|
Other_name | cewivar00285732 | |||||||
F10E9.6a.3:c.369+236A>G | ||||||||
F10E9.6c.1:c.705+236A>G | ||||||||
F10E9.6b.1:c.318+236A>G | ||||||||
F10E9.6a.2:c.369+236A>G | ||||||||
F10E9.6a.1:c.369+236A>G | ||||||||
HGVSg | CHROMOSOME_III:g.8300966A>G | |||||||
Sequence_details | SMap | S_parent | Sequence | F10E9 | ||||
Flanking_sequences | TAAAGTGAATACGAACGCCTTTTGCTCACA | TCCCCCTCTCCTTTTGCACAAGAAATTTGA | ||||||
Mapping_target | F10E9 | |||||||
Source_location | 225 | CHROMOSOME_III | 8300895 | 8300895 | From_analysis | Million_mutation_project_reanalysis | ||
Type_of_mutation | Substitution | A | G | |||||
SeqStatus | Sequenced | |||||||
Variation_type | Natural_variant | |||||||
Origin | Species | Caenorhabditis elegans | ||||||
Strain | WBStrain00006622 | From_analysis | Million_mutation_project_reanalysis | |||||
WBStrain00022852 | From_analysis | Million_mutation_project_reanalysis | ||||||
WBStrain00022856 | From_analysis | Million_mutation_project_reanalysis | ||||||
WBStrain00022878 | From_analysis | Million_mutation_project_reanalysis | ||||||
WBStrain00023286 | From_analysis | Million_mutation_project_reanalysis | ||||||
Laboratory | VC | |||||||
Analysis | Million_mutation_project_reanalysis | |||||||
Status | Live | |||||||
Affects | Gene | WBGene00003243 | ||||||
Transcript | F10E9.6a.3 | VEP_consequence | intron_variant | |||||
VEP_impact | MODIFIER | |||||||
HGVSc | F10E9.6a.3:c.369+236A>G | |||||||
Intron_number | 6/12 | |||||||
F10E9.6a.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F10E9.6a.1:c.369+236A>G | |||||||
Intron_number | 4/10 | |||||||
F10E9.6c.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F10E9.6c.1:c.705+236A>G | |||||||
Intron_number | 5/10 | |||||||
F10E9.6b.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F10E9.6b.1:c.318+236A>G | |||||||
Intron_number | 4/10 | |||||||
F10E9.6a.2 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F10E9.6a.2:c.369+236A>G | |||||||
Intron_number | 5/11 | |||||||
Method | WGS_Flibotte |