WormBase Tree Display for Variation: WBVar01551616
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WBVar01551616 | Name | Public_name | WBVar01551616 | |||||
---|---|---|---|---|---|---|---|---|
Other_name | cewivar00128673 | |||||||
T06H11.1d.1:c.293-6541T>C | ||||||||
T06H11.21:n.63A>G | ||||||||
T06H11.1f.1:c.413-6541T>C | ||||||||
T06H11.1c.1:c.148+1466T>C | ||||||||
T06H11.1b.1:c.263-6541T>C | ||||||||
HGVSg | CHROMOSOME_X:g.10115872A>G | |||||||
Sequence_details | SMap | S_parent | Sequence | T06H11 | ||||
Flanking_sequences | GGGCAACCAATTCGTAGTCTAATTAAAACT | ACTACTGAAATATTTATAAGCGGCCGCCGA | ||||||
Mapping_target | T06H11 | |||||||
Source_location | 225 | CHROMOSOME_X | 10115813 | 10115813 | From_analysis | Million_mutation_project_reanalysis | ||
Type_of_mutation | Substitution | A | G | |||||
SeqStatus | Sequenced | |||||||
Variation_type | Natural_variant | |||||||
Origin | Species | Caenorhabditis elegans | ||||||
Strain | WBStrain00004599 | From_analysis | Million_mutation_project_reanalysis | |||||
WBStrain00022850 | From_analysis | Million_mutation_project_reanalysis | ||||||
WBStrain00023072 | From_analysis | Million_mutation_project_reanalysis | ||||||
WBStrain00023139 | From_analysis | Million_mutation_project_reanalysis | ||||||
WBStrain00023192 | From_analysis | Million_mutation_project_reanalysis | ||||||
WBStrain00024204 | From_analysis | Million_mutation_project_reanalysis | ||||||
WBStrain00027647 | From_analysis | Million_mutation_project_reanalysis | ||||||
WBStrain00027648 | From_analysis | Million_mutation_project_reanalysis | ||||||
WBStrain00027660 | From_analysis | Million_mutation_project_reanalysis | ||||||
Laboratory | VC | |||||||
Analysis | Million_mutation_project_reanalysis | |||||||
Status | Live | |||||||
Affects | Gene | WBGene00202283 | ||||||
WBGene00006792 | ||||||||
Transcript | T06H11.1b.1 | VEP_consequence | intron_variant | |||||
VEP_impact | MODIFIER | |||||||
HGVSc | T06H11.1b.1:c.263-6541T>C | |||||||
Intron_number | 3/12 | |||||||
T06H11.1f.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | T06H11.1f.1:c.413-6541T>C | |||||||
Intron_number | 4/14 | |||||||
T06H11.21 | VEP_consequence | non_coding_transcript_exon_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | T06H11.21:n.63A>G | |||||||
cDNA_position | 63 | |||||||
Exon_number | 1/1 | |||||||
T06H11.1d.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | T06H11.1d.1:c.293-6541T>C | |||||||
Intron_number | 1/11 | |||||||
T06H11.1c.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | T06H11.1c.1:c.148+1466T>C | |||||||
Intron_number | 2/13 | |||||||
Method | WGS_Flibotte |