WormBase Tree Display for Variation: WBVar01830391
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WBVar01830391 | Name | Public_name | WBVar01830391 | |||||
---|---|---|---|---|---|---|---|---|
Other_name | cewivar00542502 | |||||||
F39C12.1.1:c.15090+6T>G | ||||||||
HGVSg | CHROMOSOME_X:g.4835308A>C | |||||||
Sequence_details | SMap | S_parent | Sequence | F39C12 | ||||
Flanking_sequences | TAATTTTCCGTAAGAATTTTGGTGCAAAGC | CTTACATTGCAAATGCTGAACTGCGAGAAG | ||||||
Mapping_target | F39C12 | |||||||
Source_location | 225 | CHROMOSOME_X | 4835278 | 4835278 | From_analysis | Million_mutation_project_reanalysis | ||
Type_of_mutation | Substitution | A | C | |||||
SeqStatus | Sequenced | |||||||
Variation_type | Natural_variant | |||||||
Origin | Species | Caenorhabditis elegans | ||||||
Strain | WBStrain00022886 | From_analysis | Million_mutation_project_reanalysis | |||||
Laboratory | VC | |||||||
Analysis | Million_mutation_project_reanalysis | |||||||
Status | Live | |||||||
Affects | Gene | WBGene00018193 | ||||||
Transcript | F39C12.1.1 | VEP_consequence | splice_region_variant,intron_variant | |||||
VEP_impact | LOW | |||||||
HGVSc | F39C12.1.1:c.15090+6T>G | |||||||
Intron_number | 29/30 | |||||||
Method | WGS_Flibotte |