WormBase Tree Display for Variation: WBVar01740718
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WBVar01740718 | Name | Public_name | WBVar01740718 | |||||
---|---|---|---|---|---|---|---|---|
Other_name | cewivar00439768 | |||||||
W01A11.3b.2:c.867-460G>A | ||||||||
W01A11.3b.1:c.867-460G>A | ||||||||
W01A11.3c.2:c.162-460G>A | ||||||||
W01A11.3a.1:c.1065-460G>A | ||||||||
W01A11.3c.1:c.162-460G>A | ||||||||
HGVSg | CHROMOSOME_V:g.6482303G>A | |||||||
Sequence_details | SMap | S_parent | Sequence | W01A11 | ||||
Flanking_sequences | GGACAAGTGATACGTGATATCCTACTCCCG | GGAGTCCACACCGCATACTTATTGGCCTCC | ||||||
Mapping_target | W01A11 | |||||||
Source_location | 225 | CHROMOSOME_V | 6482286 | 6482286 | From_analysis | Million_mutation_project_reanalysis | ||
Type_of_mutation | Substitution | G | A | |||||
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 | WBGene00006815 | ||||||
Transcript | W01A11.3a.1 | VEP_consequence | intron_variant | |||||
VEP_impact | MODIFIER | |||||||
HGVSc | W01A11.3a.1:c.1065-460G>A | |||||||
Intron_number | 10/17 | |||||||
W01A11.3c.2 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | W01A11.3c.2:c.162-460G>A | |||||||
Intron_number | 3/10 | |||||||
W01A11.3b.2 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | W01A11.3b.2:c.867-460G>A | |||||||
Intron_number | 9/16 | |||||||
W01A11.3b.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | W01A11.3b.1:c.867-460G>A | |||||||
Intron_number | 8/15 | |||||||
W01A11.3c.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | W01A11.3c.1:c.162-460G>A | |||||||
Intron_number | 5/12 | |||||||
Method | WGS_Flibotte |