WormBase Tree Display for Variation: WBVar01566235
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WBVar01566235 | Name | Public_name | WBVar01566235 | |||||
---|---|---|---|---|---|---|---|---|
Other_name | cewivar00150124 | |||||||
C46F11.1b.1:c.1732-18T>C | ||||||||
C46F11.1a.1:c.1747-18T>C | ||||||||
HGVSg | CHROMOSOME_III:g.3647752T>C | |||||||
Sequence_details | SMap | S_parent | Sequence | C46F11 | ||||
Flanking_sequences | ATGGTATGATGCACCATATTTGACGCGCAA | TTCATATCTCCTCTCAGGTTTGGCCACTAA | ||||||
Mapping_target | C46F11 | |||||||
Source_location | 225 | CHROMOSOME_III | 3647734 | 3647734 | From_analysis | Million_mutation_project_reanalysis | ||
Type_of_mutation | Substitution | T | C | |||||
SeqStatus | Sequenced | |||||||
Variation_type | Natural_variant | |||||||
Origin | Species | Caenorhabditis elegans | ||||||
Strain (13) | ||||||||
Laboratory | VC | |||||||
Analysis | Million_mutation_project_reanalysis | |||||||
Status | Live | |||||||
Affects | Gene | WBGene00006822 | ||||||
Transcript | C46F11.1b.1 | VEP_consequence | intron_variant | |||||
VEP_impact | MODIFIER | |||||||
HGVSc | C46F11.1b.1:c.1732-18T>C | |||||||
Intron_number | 14/16 | |||||||
C46F11.1a.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | C46F11.1a.1:c.1747-18T>C | |||||||
Intron_number | 13/16 | |||||||
Method | WGS_Flibotte |