WormBase Tree Display for Variation: WBVar01782077
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WBVar01782077 | Name | Public_name | WBVar01782077 | |||||
---|---|---|---|---|---|---|---|---|
Other_name | cewivar00482903 | |||||||
Y59A8B.13e.1:c.282+726G>C | ||||||||
Y59A8B.13d.1:c.1167+726G>C | ||||||||
Y59A8B.13c.1:c.1168-430G>C | ||||||||
Y59A8B.13a.1:c.1213-430G>C | ||||||||
Y59A8B.13f.1:c.283-430G>C | ||||||||
Y59A8B.13b.1:c.1212+726G>C | ||||||||
HGVSg | CHROMOSOME_V:g.18095130G>C | |||||||
Sequence_details | SMap | S_parent | Sequence | Y59A8B | ||||
Flanking_sequences | CACATTTGTCACCGGAGATGCGGAAGCTATGCCCAAATTTTCAATTTTTC | AGAAAATTGTATATTTTGTAAAGCAGATTA | ||||||
Mapping_target | Y59A8B | |||||||
Source_location | 225 | CHROMOSOME_V | 18095102 | 18095102 | From_analysis | Million_mutation_project_reanalysis | ||
Type_of_mutation | Substitution | G | C | |||||
SeqStatus | Sequenced | |||||||
Variation_type | Natural_variant | |||||||
Origin | Species | Caenorhabditis elegans | ||||||
Strain | WBStrain00023191 | From_analysis | Million_mutation_project_reanalysis | |||||
Laboratory | VC | |||||||
Analysis | Million_mutation_project_reanalysis | |||||||
Status | Live | |||||||
Affects | Gene | WBGene00013350 | ||||||
Transcript | Y59A8B.13b.1 | VEP_consequence | intron_variant | |||||
VEP_impact | MODIFIER | |||||||
HGVSc | Y59A8B.13b.1:c.1212+726G>C | |||||||
Intron_number | 9/10 | |||||||
Y59A8B.13f.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | Y59A8B.13f.1:c.283-430G>C | |||||||
Intron_number | 1/1 | |||||||
Y59A8B.13c.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | Y59A8B.13c.1:c.1168-430G>C | |||||||
Intron_number | 8/8 | |||||||
Y59A8B.13a.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | Y59A8B.13a.1:c.1213-430G>C | |||||||
Intron_number | 8/8 | |||||||
Y59A8B.13e.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | Y59A8B.13e.1:c.282+726G>C | |||||||
Intron_number | 1/1 | |||||||
Y59A8B.13d.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | Y59A8B.13d.1:c.1167+726G>C | |||||||
Intron_number | 9/10 | |||||||
Method | WGS_Flibotte |