WormBase Tree Display for Variation: WBVar01696089
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WBVar01696089 | Name | Public_name | WBVar01696089 | |||||
---|---|---|---|---|---|---|---|---|
Other_name | cewivar00392823 | |||||||
T24H10.7h.1:c.509+3182T>G | ||||||||
T24H10.7g.1:c.275+3182T>G | ||||||||
T24H10.7a.1:c.707+3182T>G | ||||||||
T24H10.7b.1:c.647+3182T>G | ||||||||
T24H10.7i.1:c.398+3182T>G | ||||||||
T24H10.7f.1:c.551+3182T>G | ||||||||
HGVSg | CHROMOSOME_II:g.9126518T>G | |||||||
Sequence_details | SMap | S_parent | Sequence | T24H10 | ||||
Flanking_sequences | GCAGATTGAAAATAGGTTTTCTTGGAGTTT | AAGTCATCAATTTTTTAACTTAAGTCGTTT | ||||||
Mapping_target | T24H10 | |||||||
Source_location | 225 | CHROMOSOME_II | 9126456 | 9126456 | From_analysis | Million_mutation_project_reanalysis | ||
Type_of_mutation | Substitution | T | G | |||||
SeqStatus | Sequenced | |||||||
Variation_type | Natural_variant | |||||||
Origin | Species | Caenorhabditis elegans | ||||||
Strain | WBStrain00008273 | From_analysis | Million_mutation_project_reanalysis | |||||
WBStrain00023665 | From_analysis | Million_mutation_project_reanalysis | ||||||
WBStrain00031113 | From_analysis | Million_mutation_project_reanalysis | ||||||
Laboratory | VC | |||||||
Analysis | Million_mutation_project_reanalysis | |||||||
Status | Live | |||||||
Affects | Gene | WBGene00012005 | ||||||
Transcript | T24H10.7g.1 | VEP_consequence | intron_variant | |||||
VEP_impact | MODIFIER | |||||||
HGVSc | T24H10.7g.1:c.275+3182T>G | |||||||
Intron_number | 2/3 | |||||||
T24H10.7f.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | T24H10.7f.1:c.551+3182T>G | |||||||
Intron_number | 6/8 | |||||||
T24H10.7i.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | T24H10.7i.1:c.398+3182T>G | |||||||
Intron_number | 3/4 | |||||||
T24H10.7h.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | T24H10.7h.1:c.509+3182T>G | |||||||
Intron_number | 4/5 | |||||||
T24H10.7a.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | T24H10.7a.1:c.707+3182T>G | |||||||
Intron_number | 7/9 | |||||||
T24H10.7b.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | T24H10.7b.1:c.647+3182T>G | |||||||
Intron_number | 7/9 | |||||||
Method | WGS_Flibotte |