WormBase Tree Display for Variation: WBVar02055369
expand all nodes | collapse all nodes | view schema
WBVar02055369 | Name | Public_name | WBVar02055369 | |||||
---|---|---|---|---|---|---|---|---|
Other_name | cewivar00784582 | |||||||
F56B6.2b.1:c.1827-630_1827-629insC | ||||||||
F56B6.2i.1:c.1944-630_1944-629insC | ||||||||
F56B6.2e.1:c.453-630_453-629insC | ||||||||
F56B6.2j.1:c.1947-630_1947-629insC | ||||||||
F56B6.2c.1:c.753-630_753-629insC | ||||||||
F56B6.2h.1:c.1953-630_1953-629insC | ||||||||
F56B6.2a.1:c.1938-630_1938-629insC | ||||||||
F56B6.2f.1:c.-96_-95insC | ||||||||
HGVSg | CHROMOSOME_X:g.3555810_3555811insC | |||||||
Sequence_details | SMap | S_parent | Sequence | F56B6 | ||||
Flanking_sequences | AGTGCAGTTCACCCATTACTCTTCCCATCT | CCCCCCCCCTTTTCTCCCTATTGCGCACTA | ||||||
Mapping_target | F56B6 | |||||||
Source_location | 225 | CHROMOSOME_X | 3555797 | 3555798 | From_analysis | Million_mutation_project_reanalysis | ||
Type_of_mutation | Insertion | C | ||||||
SeqStatus | Sequenced | |||||||
Variation_type | Natural_variant | |||||||
Origin | Species | Caenorhabditis elegans | ||||||
Strain | WBStrain00022930 | From_analysis | Million_mutation_project_reanalysis | |||||
Laboratory | VC | |||||||
Analysis | Million_mutation_project_reanalysis | |||||||
Status | Live | |||||||
Affects | Gene | WBGene00004350 | ||||||
Transcript | F56B6.2e.1 | VEP_consequence | intron_variant | |||||
VEP_impact | MODIFIER | |||||||
HGVSc | F56B6.2e.1:c.453-630_453-629insC | |||||||
Intron_number | 3/7 | |||||||
F56B6.2i.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F56B6.2i.1:c.1944-630_1944-629insC | |||||||
Intron_number | 12/16 | |||||||
F56B6.2a.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F56B6.2a.1:c.1938-630_1938-629insC | |||||||
Intron_number | 12/16 | |||||||
F56B6.2h.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F56B6.2h.1:c.1953-630_1953-629insC | |||||||
Intron_number | 12/16 | |||||||
F56B6.2c.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F56B6.2c.1:c.753-630_753-629insC | |||||||
Intron_number | 6/9 | |||||||
F56B6.2f.1 | VEP_consequence | 5_prime_UTR_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F56B6.2f.1:c.-96_-95insC | |||||||
cDNA_position | 29-30 | |||||||
Exon_number | 1/7 | |||||||
F56B6.2j.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F56B6.2j.1:c.1947-630_1947-629insC | |||||||
Intron_number | 11/14 | |||||||
F56B6.2b.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F56B6.2b.1:c.1827-630_1827-629insC | |||||||
Intron_number | 11/15 | |||||||
Method | WGS_Flibotte |