WormBase Tree Display for Variation: WBVar00145275
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WBVar00145275 | Evidence | Paper_evidence | WBPaper00005258 | ||
---|---|---|---|---|---|
Name | Public_name | ev708 | |||
Other_name | Y54E5B.1c.1:c.106+113_106+612del | ||||
Y54E5B.1b.3:c.106+113_106+612del | |||||
Y54E5B.1b.1:c.106+113_106+612del | |||||
Y54E5B.1a.1:c.106+113_106+612del | |||||
Y54E5B.1b.2:c.106+113_106+612del | |||||
Y54E5B.1b.4:c.106+113_106+612del | |||||
HGVSg | CHROMOSOME_I:g.14807698_14808197del | ||||
Sequence_details | SMap | S_parent | Sequence | Y54E5B | |
Flanking_sequences | actaaattcaattgaattcaatgttctatc | acgctcgagacctaatcgagtaaatatgag | |||
Mapping_target | Y54E5B | ||||
Type_of_mutation | Deletion | ||||
SeqStatus | Sequenced | ||||
Variation_type | Allele | ||||
Origin | Species | Caenorhabditis elegans | |||
Laboratory | NW | ||||
Status | Live | ||||
Affects | Gene | WBGene00004889 | |||
Transcript | Y54E5B.1b.1 | VEP_consequence | intron_variant | ||
VEP_impact | MODIFIER | ||||
HGVSc | Y54E5B.1b.1:c.106+113_106+612del | ||||
Intron_number | 2/14 | ||||
Y54E5B.1a.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | Y54E5B.1a.1:c.106+113_106+612del | ||||
Intron_number | 2/14 | ||||
Y54E5B.1b.3 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | Y54E5B.1b.3:c.106+113_106+612del | ||||
Intron_number | 2/10 | ||||
Y54E5B.1b.4 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | Y54E5B.1b.4:c.106+113_106+612del | ||||
Intron_number | 1/14 | ||||
Y54E5B.1c.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | Y54E5B.1c.1:c.106+113_106+612del | ||||
Intron_number | 2/14 | ||||
Y54E5B.1b.2 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | Y54E5B.1b.2:c.106+113_106+612del | ||||
Intron_number | 2/14 | ||||
Genetics | Interpolated_map_position | I | 27.3086 | ||
Reference | WBPaper00005258 | ||||
Method | Deletion_allele |