WormBase Tree Display for Variation: WBVar01244482
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WBVar01244482 | Evidence | Paper_evidence | WBPaper00037807 | ||||
---|---|---|---|---|---|---|---|
Name | Public_name | WBVar01244482 | |||||
Other_name | cewivar00307616 | ||||||
F45E10.1h.1:c.1411-93C>A | |||||||
F45E10.1e.1:c.151-93C>A | |||||||
F45E10.1f.1:c.487-93C>A | |||||||
F45E10.1c.1:c.1411-93C>A | |||||||
F45E10.1b.1:c.1411-93C>A | |||||||
F45E10.1a.1:c.1411-93C>A | |||||||
F45E10.1g.1:c.1411-93C>A | |||||||
F45E10.1d.1:c.1009-93C>A | |||||||
HGVSg | CHROMOSOME_II:g.11068764G>T | ||||||
Sequence_details | SMap | S_parent | Sequence | F45E10 | |||
Flanking_sequences | GAAGGCGAAGCCAGACATTAAAGTGTATCAAAATCTTAAAATCTAAAAAA | GGAAAATCTGCAACAAAAGACGACAAAAAAGGAAGAATGGAAAGACGGAA | |||||
Mapping_target | F45E10 | ||||||
Type_of_mutation | Substitution | g | T | Paper_evidence | WBPaper00037807 | ||
SeqStatus | Sequenced | ||||||
Variation_type | SNP | ||||||
Natural_variant | |||||||
Origin (6) | |||||||
Affects | Gene | WBGene00006788 | |||||
Transcript | F45E10.1b.1 | VEP_consequence | intron_variant | ||||
VEP_impact | MODIFIER | ||||||
HGVSc | F45E10.1b.1:c.1411-93C>A | ||||||
Intron_number | 10/22 | ||||||
F45E10.1a.1 | VEP_consequence | intron_variant | |||||
VEP_impact | MODIFIER | ||||||
HGVSc | F45E10.1a.1:c.1411-93C>A | ||||||
Intron_number | 11/23 | ||||||
F45E10.1f.1 | VEP_consequence | intron_variant | |||||
VEP_impact | MODIFIER | ||||||
HGVSc | F45E10.1f.1:c.487-93C>A | ||||||
Intron_number | 3/15 | ||||||
F45E10.1c.1 | VEP_consequence | intron_variant | |||||
VEP_impact | MODIFIER | ||||||
HGVSc | F45E10.1c.1:c.1411-93C>A | ||||||
Intron_number | 10/23 | ||||||
F45E10.1e.1 | VEP_consequence | intron_variant | |||||
VEP_impact | MODIFIER | ||||||
HGVSc | F45E10.1e.1:c.151-93C>A | ||||||
Intron_number | 2/14 | ||||||
F45E10.1d.1 | VEP_consequence | intron_variant | |||||
VEP_impact | MODIFIER | ||||||
HGVSc | F45E10.1d.1:c.1009-93C>A | ||||||
Intron_number | 8/20 | ||||||
F45E10.1g.1 | VEP_consequence | intron_variant | |||||
VEP_impact | MODIFIER | ||||||
HGVSc | F45E10.1g.1:c.1411-93C>A | ||||||
Intron_number | 10/21 | ||||||
F45E10.1h.1 | VEP_consequence | intron_variant | |||||
VEP_impact | MODIFIER | ||||||
HGVSc | F45E10.1h.1:c.1411-93C>A | ||||||
Intron_number | 10/21 | ||||||
Reference | WBPaper00037807 | ||||||
Method | WGS_De_Bono |