WormBase Tree Display for Variation: WBVar00143363
expand all nodes | collapse all nodes | view schema
WBVar00143363 | Evidence | Paper_evidence | WBPaper00030788 | ||||
---|---|---|---|---|---|---|---|
Name | Public_name | e642 | |||||
Other_name | C04F5.3.1:c.410-1G>A | ||||||
HGVSg | CHROMOSOME_V:g.5098267C>T | ||||||
Sequence_details | SMap | S_parent | Sequence | C04F5 | |||
Flanking_sequences | tcataagacttcatgagcaagtctctttca | gtagttctgcagtatttgaatctgataact | |||||
Mapping_target | C04F5 | ||||||
Type_of_mutation | Substitution | g | a | Paper_evidence | WBPaper00030788 | ||
SeqStatus | Sequenced | ||||||
Variation_type | Allele | ||||||
Origin (3) | |||||||
Affects | Gene | WBGene00006782 | |||||
Transcript | C04F5.3.1 | VEP_consequence | splice_acceptor_variant | ||||
VEP_impact | HIGH | ||||||
HGVSc | C04F5.3.1:c.410-1G>A | ||||||
Intron_number | 5/8 | ||||||
Genetics | Interpolated_map_position | V | -2.52014 | ||||
Reference | WBPaper00030788 | ||||||
Method | Substitution_allele |