WormBase Tree Display for Variation: WBVar01254605
expand all nodes | collapse all nodes | view schema
WBVar01254605 | Evidence | Paper_evidence | WBPaper00037807 | ||||
---|---|---|---|---|---|---|---|
Name | Public_name | WBVar01254605 | |||||
Other_name | cewivar00283530 | ||||||
F30H5.7:n.308A>G | |||||||
F30H5.6:n.122T>C | |||||||
F30H5.1.1:c.344+539T>C | |||||||
HGVSg | CHROMOSOME_III:g.492528T>C | ||||||
Sequence_details | SMap | S_parent | Sequence | F30H5 | |||
Flanking_sequences | GCGAAAAAATTTTTTTTTCAAAATTTGAGGAGGTTGGGTATGCTAAATAT | TAGCAGACCCAAGGAAAAATATTTAGCAGACCAAAGATAGGTATGCTAAA | |||||
Mapping_target | F30H5 | ||||||
Type_of_mutation | Substitution | t | C | 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 | |||||
WBStrain00023286 | From_analysis | Million_mutation_project_reanalysis | |||||
Laboratory | AX | ||||||
Analysis | WGS_De_Bono | ||||||
Million_mutation_project_reanalysis | |||||||
DB_info | Database | dbSNP_ss | ss | 539091088 | |||
Status | Live | ||||||
Affects | Gene | WBGene00198513 | |||||
WBGene00006781 | |||||||
WBGene00197590 | |||||||
Transcript | F30H5.7 | VEP_consequence | non_coding_transcript_exon_variant | ||||
VEP_impact | MODIFIER | ||||||
HGVSc | F30H5.7:n.308A>G | ||||||
cDNA_position | 308 | ||||||
Exon_number | 1/1 | ||||||
F30H5.6 | VEP_consequence | non_coding_transcript_exon_variant | |||||
VEP_impact | MODIFIER | ||||||
HGVSc | F30H5.6:n.122T>C | ||||||
cDNA_position | 122 | ||||||
Exon_number | 1/1 | ||||||
F30H5.1.1 | VEP_consequence | intron_variant | |||||
VEP_impact | MODIFIER | ||||||
HGVSc | F30H5.1.1:c.344+539T>C | ||||||
Intron_number | 4/12 | ||||||
Reference | WBPaper00037807 | ||||||
Method | WGS_De_Bono |