WormBase Tree Display for Variation: WBVar01975611
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WBVar01975611 | Name | Public_name | WBVar01975611 | |||||
---|---|---|---|---|---|---|---|---|
Other_name | cewivar00701612 | |||||||
C01G10.11b.1:c.*48_*49del | ||||||||
C01G10.11f.1:c.1072+116_1072+117del | ||||||||
C01G10.11e.1:c.268+116_268+117del | ||||||||
C01G10.11d.1:c.622+116_622+117del | ||||||||
C01G10.11c.1:c.769+116_769+117del | ||||||||
C01G10.11a.1:c.1042+116_1042+117del | ||||||||
HGVSg | CHROMOSOME_V:g.15078837_15078838del | |||||||
Sequence_details | SMap | S_parent | Sequence | C01G10 | ||||
Flanking_sequences | AGATATTTGCATAAGAGATACAGAATTTTA | ATGTTTTTCTCGGGATTATGTCCCCTTGTT | ||||||
Mapping_target | C01G10 | |||||||
Source_location | 225 | CHROMOSOME_V | 15078820 | 15078821 | From_analysis | Million_mutation_project_reanalysis | ||
Type_of_mutation | Deletion | |||||||
SeqStatus | Sequenced | |||||||
Variation_type | Natural_variant | |||||||
Origin | Species | Caenorhabditis elegans | ||||||
Strain | WBStrain00004602 | From_analysis | Million_mutation_project_reanalysis | |||||
WBStrain00022930 | From_analysis | Million_mutation_project_reanalysis | ||||||
WBStrain00023286 | From_analysis | Million_mutation_project_reanalysis | ||||||
Laboratory | VC | |||||||
Analysis | Million_mutation_project_reanalysis | |||||||
Status | Live | |||||||
Affects | Gene | WBGene00006808 | ||||||
WBGene00305285 | ||||||||
Transcript | C01G10.11f.1 | VEP_consequence | intron_variant | |||||
VEP_impact | MODIFIER | |||||||
HGVSc | C01G10.11f.1:c.1072+116_1072+117del | |||||||
Intron_number | 10/11 | |||||||
C01G10.11d.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | C01G10.11d.1:c.622+116_622+117del | |||||||
Intron_number | 4/4 | |||||||
C01G10.11e.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | C01G10.11e.1:c.268+116_268+117del | |||||||
Intron_number | 2/2 | |||||||
C01G10.11b.1 | VEP_consequence | 3_prime_UTR_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | C01G10.11b.1:c.*48_*49del | |||||||
cDNA_position | 1169-1170 | |||||||
Exon_number | 10/10 | |||||||
C01G10.11a.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | C01G10.11a.1:c.1042+116_1042+117del | |||||||
Intron_number | 9/10 | |||||||
C25D7.19 | ||||||||
C01G10.11c.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | C01G10.11c.1:c.769+116_769+117del | |||||||
Intron_number | 6/6 | |||||||
Method | WGS_Flibotte |