WormBase Tree Display for Variation: WBVar01255526
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WBVar01255526 | Evidence | Paper_evidence | WBPaper00037807 | ||||
---|---|---|---|---|---|---|---|
Name | Public_name | WBVar01255526 | |||||
Other_name | cewivar00283785 | ||||||
T12B5.8.2:c.114-497G>A | |||||||
T12B5.9:n.579G>A | |||||||
T12B5.8.1:c.114-497G>A | |||||||
HGVSg | CHROMOSOME_III:g.942254C>T | ||||||
Sequence_details | SMap | S_parent | Sequence | T12B5 | |||
Flanking_sequences | ACCGCGAAGTGTATTGGGTGCTTTTCTTGGACTGCAAGAGCGAGCGAGTT | AGCTGATCAGAAAAGGTGGAAGCCGTGATTGTTCTGTCTTGCGGAAGCAA | |||||
Mapping_target | T12B5 | ||||||
Type_of_mutation | Substitution | c | T | Paper_evidence | WBPaper00037807 | ||
SeqStatus | Sequenced | ||||||
Variation_type | SNP | ||||||
Natural_variant | |||||||
Origin | Species | Caenorhabditis elegans | |||||
Strain | WBStrain00006622 | From_analysis | Million_mutation_project_reanalysis | ||||
WBStrain00006640 | From_analysis | Million_mutation_project_reanalysis | |||||
WBStrain00006642 | From_analysis | WGS_De_Bono | |||||
WBStrain00006643 | From_analysis | Million_mutation_project_reanalysis | |||||
WBStrain00006645 | From_analysis | Million_mutation_project_reanalysis | |||||
WBStrain00022852 | From_analysis | Million_mutation_project_reanalysis | |||||
WBStrain00022878 | From_analysis | Million_mutation_project_reanalysis | |||||
WBStrain00027647 | From_analysis | Million_mutation_project_reanalysis | |||||
Laboratory | AX | ||||||
Analysis | WGS_De_Bono | ||||||
Million_mutation_project_reanalysis | |||||||
DB_info | Database | dbSNP_ss | ss | 539091917 | |||
Status | Live | ||||||
Affects | Gene | WBGene00023345 | |||||
WBGene00020455 | |||||||
Transcript | T12B5.8.2 | VEP_consequence | intron_variant | ||||
VEP_impact | MODIFIER | ||||||
HGVSc | T12B5.8.2:c.114-497G>A | ||||||
Intron_number | 2/6 | ||||||
T12B5.8.1 | VEP_consequence | intron_variant | |||||
VEP_impact | MODIFIER | ||||||
HGVSc | T12B5.8.1:c.114-497G>A | ||||||
Intron_number | 2/5 | ||||||
Pseudogene | T12B5.9 | VEP_consequence | non_coding_transcript_exon_variant | ||||
VEP_impact | MODIFIER | ||||||
HGVSc | T12B5.9:n.579G>A | ||||||
cDNA_position | 579 | ||||||
Exon_number | 5/7 | ||||||
Reference | WBPaper00037807 | ||||||
Method | WGS_De_Bono |