WormBase Tree Display for Variation: WBVar02066045
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WBVar02066045 | Name | Public_name | WBVar02066045 | |||||
---|---|---|---|---|---|---|---|---|
Other_name | cewivar00795286 | |||||||
T05A10.1c.1:c.-1612+1790_-1612+1791insT | ||||||||
T05A10.1m.1:c.108+1790_108+1791insT | ||||||||
T05A10.1b.1:c.108+1790_108+1791insT | ||||||||
HGVSg | CHROMOSOME_X:g.10771191_10771192insT | |||||||
Sequence_details | SMap | S_parent | Sequence | T05A10 | ||||
Flanking_sequences | GCCTCTTTTCAAACTCCTCGGGGTGTTTCC | TTTTTTTTTCCTCTCTCTCTTTTTTTCTGT | ||||||
Mapping_target | T05A10 | |||||||
Source_location | 225 | CHROMOSOME_X | 10771126 | 10771127 | From_analysis | Million_mutation_project_reanalysis | ||
Type_of_mutation | Insertion | T | ||||||
SeqStatus | Sequenced | |||||||
Variation_type | Natural_variant | |||||||
Origin (5) | ||||||||
Affects | Gene | WBGene00004862 | ||||||
Transcript | T05A10.1m.1 | VEP_consequence | intron_variant | |||||
VEP_impact | MODIFIER | |||||||
HGVSc | T05A10.1m.1:c.108+1790_108+1791insT | |||||||
Intron_number | 2/26 | |||||||
T05A10.1b.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | T05A10.1b.1:c.108+1790_108+1791insT | |||||||
Intron_number | 2/8 | |||||||
T05A10.1c.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | T05A10.1c.1:c.-1612+1790_-1612+1791insT | |||||||
Intron_number | 1/27 | |||||||
Method | WGS_Flibotte |