WormBase Tree Display for Variation: WBVar00266983
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WBVar00266983 | Evidence | Paper_evidence | WBPaper00005369 | ||
---|---|---|---|---|---|
Name | Public_name | WBVar00266983 | |||
Other_name (11) | |||||
HGVSg | CHROMOSOME_I:g.4080035dup | ||||
Sequence_details | SMap | S_parent | Sequence | C24G7 | |
Flanking_sequences | AAAATTACGAGTGCCAAATGCTGGCACTTAATAACTAAACATTGCGTAAAGTAAACAATTTTTAATTTGAATATAAAAGATCATCTCGCTAATTTTTTTT | CTTCGAGAAGTTACAGGAAAATTGAAAGATGTCTACAATATTTATTCTGAATCCAAAGTAAGCCAATAATTTTTTTTTAATTCTGGCGATGCTTCACCGTC | |||
Mapping_target | C24G7 | ||||
Type_of_mutation | Insertion | T | |||
SeqStatus | Sequenced | ||||
Variation_type | SNP | ||||
Predicted_SNP | |||||
Natural_variant | |||||
Origin | Species | Caenorhabditis elegans | |||
Strain | WBStrain00004602 | From_analysis | SNP_Swan | ||
Analysis | SNP_Swan | ||||
Status | Live | ||||
Affects | Gene | WBGene00006820 | |||
Transcript | C09D1.1b.1 | VEP_consequence | intron_variant | ||
VEP_impact | MODIFIER | ||||
HGVSc | C09D1.1b.1:c.20087+319dup | ||||
Intron_number | 35/48 | ||||
C09D1.1p.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | C09D1.1p.1:c.16508+319dup | ||||
Intron_number | 25/37 | ||||
C09D1.1j.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | C09D1.1j.1:c.16748+319dup | ||||
Intron_number | 24/36 | ||||
C09D1.1g.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | C09D1.1g.1:c.18668+319dup | ||||
Intron_number | 26/38 | ||||
C09D1.1k.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | C09D1.1k.1:c.20021+319dup | ||||
Intron_number | 34/46 | ||||
C09D1.1i.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | C09D1.1i.1:c.18602+319dup | ||||
Intron_number | 25/37 | ||||
C09D1.1n.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | C09D1.1n.1:c.17927+319dup | ||||
Intron_number | 34/46 | ||||
C09D1.1h.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | C09D1.1h.1:c.16949+319dup | ||||
Intron_number | 26/38 | ||||
C09D1.1f.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | C09D1.1f.1:c.18167+319dup | ||||
Intron_number | 33/45 | ||||
C09D1.1m.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | C09D1.1m.1:c.18368+319dup | ||||
Intron_number | 35/47 | ||||
Reference | WBPaper00005369 | ||||
Method | SNP_Swan |