WormBase Tree Display for Variation: WBVar00054302
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WBVar00054302 | Evidence | Paper_evidence | WBPaper00005344 | ||||
---|---|---|---|---|---|---|---|
Name | Public_name | cs30 | |||||
Other_name | C44H4.7c.1:c.2499+1G>A | ||||||
C44H4.7b.1:c.2493+1G>A | |||||||
C44H4.7a.1:c.2538+1G>A | |||||||
C44H4.7d.1:c.741+1G>A | |||||||
HGVSg | CHROMOSOME_X:g.14608019G>A | ||||||
Sequence_details | SMap | S_parent | Sequence | F54E4 | |||
Flanking_sequences | tcatcatttcactgctttacaaagtgtcag | tacagtaaatataataagatagggaaagga | |||||
Mapping_target | F54E4 | ||||||
Type_of_mutation | Substitution | g | a | Paper_evidence | WBPaper00005344 | ||
SeqStatus | Sequenced | ||||||
Variation_type | Allele | ||||||
Origin | Species | Caenorhabditis elegans | |||||
Laboratory | UP | ||||||
Status | Live | ||||||
Affects | Gene | WBGene00001325 | |||||
Transcript | C44H4.7c.1 | VEP_consequence | splice_donor_variant | ||||
VEP_impact | HIGH | ||||||
HGVSc | C44H4.7c.1:c.2499+1G>A | ||||||
Intron_number | 15/17 | ||||||
C44H4.7b.1 | VEP_consequence | splice_donor_variant | |||||
VEP_impact | HIGH | ||||||
HGVSc | C44H4.7b.1:c.2493+1G>A | ||||||
Intron_number | 15/17 | ||||||
C44H4.7a.1 | VEP_consequence | splice_donor_variant | |||||
VEP_impact | HIGH | ||||||
HGVSc | C44H4.7a.1:c.2538+1G>A | ||||||
Intron_number | 16/18 | ||||||
C44H4.7d.1 | VEP_consequence | splice_donor_variant | |||||
VEP_impact | HIGH | ||||||
HGVSc | C44H4.7d.1:c.741+1G>A | ||||||
Intron_number | 5/6 | ||||||
Interactor (21) | |||||||
Genetics | Interpolated_map_position | X | 18.7008 | ||||
Reference | WBPaper00005344 | ||||||
Method | Substitution_allele |