WormBase Tree Display for Variation: WBVar01626908
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WBVar01626908 | Name | Public_name | WBVar01626908 | |||||
---|---|---|---|---|---|---|---|---|
Other_name | cewivar00307086 | |||||||
C41C4.5a.1:c.457+54G>A | ||||||||
C41C4.5d.1:c.715+54G>A | ||||||||
C41C4.5e.1:c.715+54G>A | ||||||||
C41C4.4a.1:c.801+3339C>T | ||||||||
C41C4.5c.2:c.397+54G>A | ||||||||
C41C4.5b.1:c.571+54G>A | ||||||||
C41C4.5h.1:c.715+54G>A | ||||||||
C41C4.5c.1:c.397+54G>A | ||||||||
HGVSg | CHROMOSOME_II:g.8119572G>A | |||||||
Sequence_details | SMap | S_parent | Sequence | C41C4 | ||||
Flanking_sequences | TGACAAATTGTTTTAAAAAACCTTTCACAG | GTAAAGATTTTTGAAATTCTAAATATAAAA | ||||||
Mapping_target | C41C4 | |||||||
Source_location | 225 | CHROMOSOME_II | 8119520 | 8119520 | From_analysis | Million_mutation_project_reanalysis | ||
Type_of_mutation | Substitution | G | A | |||||
SeqStatus | Sequenced | |||||||
Variation_type | Natural_variant | |||||||
Origin | Species | Caenorhabditis elegans | ||||||
Strain | WBStrain00006625 | From_analysis | Million_mutation_project_reanalysis | |||||
WBStrain00023139 | From_analysis | Million_mutation_project_reanalysis | ||||||
WBStrain00027648 | From_analysis | Million_mutation_project_reanalysis | ||||||
WBStrain00027652 | 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 | WBGene00002147 | ||||||
WBGene00006832 | ||||||||
Transcript | C41C4.5e.1 | VEP_consequence | intron_variant | |||||
VEP_impact | MODIFIER | |||||||
HGVSc | C41C4.5e.1:c.715+54G>A | |||||||
Intron_number | 6/15 | |||||||
C41C4.4a.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | C41C4.4a.1:c.801+3339C>T | |||||||
Intron_number | 6/11 | |||||||
C41C4.5c.2 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | C41C4.5c.2:c.397+54G>A | |||||||
Intron_number | 7/14 | |||||||
C41C4.5c.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | C41C4.5c.1:c.397+54G>A | |||||||
Intron_number | 6/15 | |||||||
C41C4.5d.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | C41C4.5d.1:c.715+54G>A | |||||||
Intron_number | 6/13 | |||||||
C41C4.5a.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | C41C4.5a.1:c.457+54G>A | |||||||
Intron_number | 5/14 | |||||||
C41C4.5h.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | C41C4.5h.1:c.715+54G>A | |||||||
Intron_number | 5/14 | |||||||
C41C4.5b.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | C41C4.5b.1:c.571+54G>A | |||||||
Intron_number | 5/14 | |||||||
Method | WGS_Flibotte |