WormBase Tree Display for Variation: WBVar01729848
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WBVar01729848 | Name | Public_name | WBVar01729848 | |||||
---|---|---|---|---|---|---|---|---|
Other_name (11) | ||||||||
HGVSg | CHROMOSOME_IV:g.7441733T>C | |||||||
Sequence_details | SMap | S_parent | Sequence | B0496 | ||||
Flanking_sequences | GGTTCTAGAATAATCCAGAATTTTTTCGAA | TTTCCAGAAGGTTCTAAAGCTTTTCAGAAA | ||||||
Mapping_target | B0496 | |||||||
Source_location | 225 | CHROMOSOME_IV | 7441722 | 7441722 | From_analysis | Million_mutation_project_reanalysis | ||
Type_of_mutation | Substitution | T | C | |||||
SeqStatus | Sequenced | |||||||
Variation_type | Natural_variant | |||||||
Origin | Species | Caenorhabditis elegans | ||||||
Strain | WBStrain00023139 | From_analysis | Million_mutation_project_reanalysis | |||||
WBStrain00027648 | From_analysis | Million_mutation_project_reanalysis | ||||||
WBStrain00027660 | From_analysis | Million_mutation_project_reanalysis | ||||||
WBStrain00027662 | From_analysis | Million_mutation_project_reanalysis | ||||||
Laboratory | VC | |||||||
Analysis | Million_mutation_project_reanalysis | |||||||
Status | Live | |||||||
Affects | Gene | WBGene00006814 | ||||||
Transcript | B0496.3h.2 | VEP_consequence | intron_variant | |||||
VEP_impact | MODIFIER | |||||||
HGVSc | B0496.3h.2:c.3319-301T>C | |||||||
Intron_number | 19/27 | |||||||
B0496.3a.2 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | B0496.3a.2:c.3388-301T>C | |||||||
Intron_number | 20/27 | |||||||
B0496.3b.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | B0496.3b.1:c.3583-301T>C | |||||||
Intron_number | 21/30 | |||||||
B0496.3i.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | B0496.3i.1:c.3634-301T>C | |||||||
Intron_number | 21/29 | |||||||
B0496.3g.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | B0496.3g.1:c.3319-301T>C | |||||||
Intron_number | 22/31 | |||||||
B0496.3a.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | B0496.3a.1:c.3388-301T>C | |||||||
Intron_number | 25/32 | |||||||
B0496.3e.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | B0496.3e.1:c.4228-301T>C | |||||||
Intron_number | 26/34 | |||||||
B0496.3f.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | B0496.3f.1:c.3436-301T>C | |||||||
Intron_number | 20/28 | |||||||
B0496.3h.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | B0496.3h.1:c.3319-301T>C | |||||||
Intron_number | 22/30 | |||||||
B0496.3d.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | B0496.3d.1:c.3511-301T>C | |||||||
Intron_number | 23/32 | |||||||
Method | WGS_Flibotte |