WormBase Tree Display for Variation: WBVar01544418
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WBVar01544418 | Name | Public_name | WBVar01544418 | |||||
---|---|---|---|---|---|---|---|---|
Other_name | cewivar00115231 | |||||||
F25C8.3e.1:c.2825+176T>G | ||||||||
F25C8.3d.1:c.2825+176T>G | ||||||||
F25C8.3b.1:c.2825+176T>G | ||||||||
F25C8.3a.1:c.2825+176T>G | ||||||||
F25C8.3c.1:c.2771+176T>G | ||||||||
HGVSg | CHROMOSOME_V:g.20886877T>G | |||||||
Sequence_details | SMap | S_parent | Sequence | F25C8 | ||||
Flanking_sequences | CGGTCAAAGTTTTGGCACATTGCCAAAATT | TGAAAAATATGAGCTTTTTAGAAAATCCGA | ||||||
Mapping_target | F25C8 | |||||||
Source_location | 225 | CHROMOSOME_V | 20886846 | 20886846 | From_analysis | Million_mutation_project_reanalysis | ||
Type_of_mutation | Substitution | T | G | |||||
SeqStatus | Sequenced | |||||||
Variation_type | Natural_variant | |||||||
Origin | Species | Caenorhabditis elegans | ||||||
Strain (21) | ||||||||
Laboratory | VC | |||||||
Analysis | Million_mutation_project_reanalysis | |||||||
Status | Live | |||||||
Affects | Gene | WBGene00006812 | ||||||
Transcript | F25C8.3d.1 | VEP_consequence | intron_variant | |||||
VEP_impact | MODIFIER | |||||||
HGVSc | F25C8.3d.1:c.2825+176T>G | |||||||
Intron_number | 13/36 | |||||||
F25C8.3b.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F25C8.3b.1:c.2825+176T>G | |||||||
Intron_number | 14/35 | |||||||
F25C8.3e.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F25C8.3e.1:c.2825+176T>G | |||||||
Intron_number | 13/33 | |||||||
F25C8.3c.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F25C8.3c.1:c.2771+176T>G | |||||||
Intron_number | 13/34 | |||||||
F25C8.3a.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F25C8.3a.1:c.2825+176T>G | |||||||
Intron_number | 13/36 | |||||||
Method | WGS_Flibotte |