WormBase Tree Display for Variation: WBVar01604549
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WBVar01604549 | Name | Public_name | WBVar01604549 | |||||
---|---|---|---|---|---|---|---|---|
Other_name | cewivar00281238 | |||||||
F52H3.1.4:c.2092+709T>C | ||||||||
F52H3.1.3:c.2092+709T>C | ||||||||
F52H3.1.1:c.2092+709T>C | ||||||||
F52H3.1.2:c.2092+709T>C | ||||||||
HGVSg | CHROMOSOME_II:g.10034520A>G | |||||||
Sequence_details | SMap | S_parent | Sequence | F52H3 | ||||
Flanking_sequences | GAAACAATTTTCCATACTCAGGTTATCCAA | TTTCGCCATGATTTTTCTTACTTAATTTAA | ||||||
Mapping_target | F52H3 | |||||||
Source_location | 225 | CHROMOSOME_II | 10034461 | 10034461 | 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 | ||||||
WBStrain00022902 | From_analysis | Million_mutation_project_reanalysis | ||||||
WBStrain00022930 | From_analysis | Million_mutation_project_reanalysis | ||||||
WBStrain00023018 | From_analysis | Million_mutation_project_reanalysis | ||||||
WBStrain00023072 | From_analysis | Million_mutation_project_reanalysis | ||||||
WBStrain00023191 | From_analysis | Million_mutation_project_reanalysis | ||||||
Laboratory | VC | |||||||
Analysis | Million_mutation_project_reanalysis | |||||||
Status | Live | |||||||
Affects | Gene | WBGene00002497 | ||||||
Transcript | F52H3.1.3 | VEP_consequence | intron_variant | |||||
VEP_impact | MODIFIER | |||||||
HGVSc | F52H3.1.3:c.2092+709T>C | |||||||
Intron_number | 10/11 | |||||||
F52H3.1.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F52H3.1.1:c.2092+709T>C | |||||||
Intron_number | 10/11 | |||||||
F52H3.1.2 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F52H3.1.2:c.2092+709T>C | |||||||
Intron_number | 10/11 | |||||||
F52H3.1.4 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F52H3.1.4:c.2092+709T>C | |||||||
Intron_number | 9/10 | |||||||
Method | WGS_Flibotte |