WormBase Tree Display for Variation: WBVar01533957
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WBVar01533957 | Name | Public_name | WBVar01533957 | |||||
---|---|---|---|---|---|---|---|---|
Other_name | cewivar00080062 | |||||||
F56D12.1c.1:c.1137+21C>G | ||||||||
F56D12.1b.1:c.1137+21C>G | ||||||||
F56D12.1d.1:c.717+21C>G | ||||||||
F56D12.1a.2:c.1137+21C>G | ||||||||
F56D12.1a.1:c.1137+21C>G | ||||||||
HGVSg | CHROMOSOME_II:g.1307536G>C | |||||||
Sequence_details | SMap | S_parent | Sequence | F56D12 | ||||
Flanking_sequences | ACCTGTAAACTACAAACTACACAAAAATCG | CAAGCCAAACAGTGGCCTACATCTCCAAGC | ||||||
Mapping_target | F56D12 | |||||||
Source_location | 225 | CHROMOSOME_II | 1307543 | 1307543 | From_analysis | Million_mutation_project_reanalysis | ||
Type_of_mutation | Substitution | G | C | |||||
SeqStatus | Sequenced | |||||||
Variation_type | Natural_variant | |||||||
Origin | Species | Caenorhabditis elegans | ||||||
Strain | WBStrain00000034 | From_analysis | Million_mutation_project_reanalysis | |||||
WBStrain00004599 | From_analysis | Million_mutation_project_reanalysis | ||||||
WBStrain00006625 | From_analysis | Million_mutation_project_reanalysis | ||||||
WBStrain00023665 | From_analysis | Million_mutation_project_reanalysis | ||||||
WBStrain00027652 | From_analysis | Million_mutation_project_reanalysis | ||||||
Laboratory | VC | |||||||
Analysis | Million_mutation_project_reanalysis | |||||||
Status | Live | |||||||
Affects | Gene | WBGene00000112 | ||||||
Transcript | F56D12.1b.1 | VEP_consequence | intron_variant | |||||
VEP_impact | MODIFIER | |||||||
HGVSc | F56D12.1b.1:c.1137+21C>G | |||||||
Intron_number | 6/7 | |||||||
F56D12.1a.2 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F56D12.1a.2:c.1137+21C>G | |||||||
Intron_number | 7/9 | |||||||
F56D12.1a.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F56D12.1a.1:c.1137+21C>G | |||||||
Intron_number | 6/8 | |||||||
F56D12.1d.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F56D12.1d.1:c.717+21C>G | |||||||
Intron_number | 2/3 | |||||||
F56D12.1c.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F56D12.1c.1:c.1137+21C>G | |||||||
Intron_number | 5/5 | |||||||
Method | WGS_Flibotte |