WormBase Tree Display for Variation: WBVar01729839
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WBVar01729839 | Name | Public_name | WBVar01729839 | |||||
---|---|---|---|---|---|---|---|---|
Other_name | cewivar00428364 | |||||||
B0496.12:n.42A>G | ||||||||
B0496.3e.1:c.710-211T>C | ||||||||
B0496.3h.1:c.-8-211T>C | ||||||||
B0496.19:n.249T>C | ||||||||
B0496.3g.1:c.-8-211T>C | ||||||||
B0496.3d.1:c.-8-211T>C | ||||||||
B0496.3a.1:c.-8-211T>C | ||||||||
HGVSg | CHROMOSOME_IV:g.7428715T>C | |||||||
Sequence_details | SMap | S_parent | Sequence | B0496 | ||||
Flanking_sequences | CATTATTATCATCGAGAGCCCCCACTTTCT | TTCTTATATTTTCAAATTTCAATCGTTTAT | ||||||
Mapping_target | B0496 | |||||||
Source_location | 225 | CHROMOSOME_IV | 7428704 | 7428704 | From_analysis | Million_mutation_project_reanalysis | ||
Type_of_mutation | Substitution | T | C | |||||
SeqStatus | Sequenced | |||||||
Variation_type | Natural_variant | |||||||
Origin | Species | Caenorhabditis elegans | ||||||
Strain | WBStrain00023139 | From_analysis | Million_mutation_project_reanalysis | |||||
WBStrain00027648 | From_analysis | Million_mutation_project_reanalysis | ||||||
WBStrain00027660 | From_analysis | Million_mutation_project_reanalysis | ||||||
WBStrain00027662 | From_analysis | Million_mutation_project_reanalysis | ||||||
Laboratory | VC | |||||||
Analysis | Million_mutation_project_reanalysis | |||||||
Status | Live | |||||||
Affects | Gene | WBGene00201851 | ||||||
WBGene00195793 | ||||||||
WBGene00006814 | ||||||||
Transcript | B0496.3e.1 | VEP_consequence | intron_variant | |||||
VEP_impact | MODIFIER | |||||||
HGVSc | B0496.3e.1:c.710-211T>C | |||||||
Intron_number | 6/34 | |||||||
B0496.12 | VEP_consequence | non_coding_transcript_exon_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | B0496.12:n.42A>G | |||||||
cDNA_position | 42 | |||||||
Exon_number | 1/1 | |||||||
B0496.3h.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | B0496.3h.1:c.-8-211T>C | |||||||
Intron_number | 2/30 | |||||||
B0496.3d.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | B0496.3d.1:c.-8-211T>C | |||||||
Intron_number | 2/32 | |||||||
B0496.19 | VEP_consequence | non_coding_transcript_exon_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | B0496.19:n.249T>C | |||||||
cDNA_position | 249 | |||||||
Exon_number | 1/1 | |||||||
B0496.3g.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | B0496.3g.1:c.-8-211T>C | |||||||
Intron_number | 2/31 | |||||||
B0496.3a.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | B0496.3a.1:c.-8-211T>C | |||||||
Intron_number | 5/32 | |||||||
Method | WGS_Flibotte |