WormBase Tree Display for Variation: WBVar01895353
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WBVar01895353 | Name | Public_name | WBVar01895353 | |||||
---|---|---|---|---|---|---|---|---|
Other_name | cewivar00610672 | |||||||
F45E10.1h.1:c.1114-249C>A | ||||||||
F45E10.1c.1:c.1114-249C>A | ||||||||
F45E10.1a.1:c.1114-249C>A | ||||||||
F45E10.1b.1:c.1114-249C>A | ||||||||
F45E10.1f.1:c.190-249C>A | ||||||||
F45E10.1g.1:c.1114-249C>A | ||||||||
F45E10.1d.1:c.712-249C>A | ||||||||
HGVSg | CHROMOSOME_II:g.11070073G>T | |||||||
Sequence_details | SMap | S_parent | Sequence | F45E10 | ||||
Flanking_sequences | TTTTTCAAAAAGTGCATCTCACACAAAAAT | TTTTGCAATTTGTGCTCTTTCACTCTGTAG | ||||||
Mapping_target | F45E10 | |||||||
Source_location | 225 | CHROMOSOME_II | 11070015 | 11070015 | From_analysis | Million_mutation_project_reanalysis | ||
Type_of_mutation | Substitution | G | T | |||||
SeqStatus | Sequenced | |||||||
Variation_type | Natural_variant | |||||||
Origin | Species | Caenorhabditis elegans | ||||||
Strain | WBStrain00024204 | From_analysis | Million_mutation_project_reanalysis | |||||
Laboratory | VC | |||||||
Analysis | Million_mutation_project_reanalysis | |||||||
Status | Live | |||||||
Affects | Gene | WBGene00006788 | ||||||
Transcript | F45E10.1c.1 | VEP_consequence | intron_variant | |||||
VEP_impact | MODIFIER | |||||||
HGVSc | F45E10.1c.1:c.1114-249C>A | |||||||
Intron_number | 8/23 | |||||||
F45E10.1b.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F45E10.1b.1:c.1114-249C>A | |||||||
Intron_number | 8/22 | |||||||
F45E10.1d.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F45E10.1d.1:c.712-249C>A | |||||||
Intron_number | 6/20 | |||||||
F45E10.1g.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F45E10.1g.1:c.1114-249C>A | |||||||
Intron_number | 8/21 | |||||||
F45E10.1a.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F45E10.1a.1:c.1114-249C>A | |||||||
Intron_number | 9/23 | |||||||
F45E10.1h.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F45E10.1h.1:c.1114-249C>A | |||||||
Intron_number | 8/21 | |||||||
F45E10.1f.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F45E10.1f.1:c.190-249C>A | |||||||
Intron_number | 1/15 | |||||||
Method | WGS_Flibotte |