WormBase Tree Display for Variation: WBVar00273004
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WBVar00273004 | Evidence | Paper_evidence | WBPaper00005369 | ||
---|---|---|---|---|---|
Name | Public_name | WBVar00273004 | |||
Other_name | uCE5-2455 | ||||
cewivar00702627 | |||||
T25E12.4a.1:c.2101+7375_2101+7376insAAT | |||||
T25E12.4d.1:c.1435+7375_1435+7376insAAT | |||||
T25E12.4e.1:c.2095+7375_2095+7376insAAT | |||||
T25E12.4f.1:c.2176+7375_2176+7376insAAT | |||||
T25E12.4c.1:c.1507+7375_1507+7376insAAT | |||||
HGVSg | CHROMOSOME_V:g.16777186_16777187insAAT | ||||
Sequence_details | SMap | S_parent | Sequence | F14D1 | |
Flanking_sequences | AGAATGGCAGTTCGCGAAGTGGCGCGGTTTTTTTTGTCAAATTTTCTTGAAATTCATTAGAACGGCGTATAAATAGCTTTAAACATTCCCAGAGCTCCCAA | TTTTTTCTGGAATAAAAAAAAGTAATTTTTCGACCTCGCTATCAACATGTTTTCAGAGCCAAAACGTCATTCAAATGAATATTTCATTCTGTCGCTTTTA | |||
Mapping_target | F14D1 | ||||
Type_of_mutation | Insertion | AAT | |||
SeqStatus | Sequenced | ||||
Variation_type | SNP | ||||
Predicted_SNP | |||||
Natural_variant | |||||
Origin | Species | Caenorhabditis elegans | |||
Strain | WBStrain00004602 | From_analysis | SNP_Swan | ||
Million_mutation_project_reanalysis | |||||
Analysis | SNP_Swan | ||||
Million_mutation_project_reanalysis | |||||
History | Acquires_merge | WBVar01976619 | |||
Status | Live | ||||
Affects | Gene | WBGene00012019 | |||
Transcript | T25E12.4f.1 | VEP_consequence | intron_variant | ||
VEP_impact | MODIFIER | ||||
HGVSc | T25E12.4f.1:c.2176+7375_2176+7376insAAT | ||||
Intron_number | 15/18 | ||||
T25E12.4d.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | T25E12.4d.1:c.1435+7375_1435+7376insAAT | ||||
Intron_number | 10/13 | ||||
T25E12.4c.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | T25E12.4c.1:c.1507+7375_1507+7376insAAT | ||||
Intron_number | 10/13 | ||||
T25E12.4a.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | T25E12.4a.1:c.2101+7375_2101+7376insAAT | ||||
Intron_number | 14/18 | ||||
T25E12.4e.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | T25E12.4e.1:c.2095+7375_2095+7376insAAT | ||||
Intron_number | 14/17 | ||||
Reference | WBPaper00005369 | ||||
Method | SNP_Swan |