WormBase Tree Display for Variation: WBVar00652896
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WBVar00652896 | Name | Public_name | gk775770 | ||
---|---|---|---|---|---|
Other_name | C54G4.7.2:c.389+119C>T | ||||
C54G4.7.3:c.389+119C>T | |||||
C54G4.7.1:c.389+119C>T | |||||
HGVSg | CHROMOSOME_I:g.8021478C>T | ||||
Sequence_details | SMap | S_parent | Sequence | C54G4 | |
Flanking_sequences | TTTAAAACTCGCTGCAGAGTTTTTAACTTACAGTTTCCTTTAAAGGCGCA | ACCTTTTTGCATTTAACAAAATTCATCGTGTCGAGACCGGATACCGTATT | |||
Mapping_target | C54G4 | ||||
Type_of_mutation | Substitution | C | T | ||
SeqStatus | Sequenced | ||||
Variation_type | Allele | ||||
Origin | Species | Caenorhabditis elegans | |||
Strain | WBStrain00039688 | ||||
Laboratory | VC | ||||
Analysis | Million_Mutation_Project | ||||
Status | Live | ||||
Affects | Gene | WBGene00008317 | |||
Transcript | C54G4.7.1 | VEP_consequence | intron_variant | ||
VEP_impact | MODIFIER | ||||
HGVSc | C54G4.7.1:c.389+119C>T | ||||
Intron_number | 6/7 | ||||
C54G4.7.3 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | C54G4.7.3:c.389+119C>T | ||||
Intron_number | 4/5 | ||||
C54G4.7.2 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | C54G4.7.2:c.389+119C>T | ||||
Intron_number | 5/6 | ||||
Reference | WBPaper00042537 | ||||
Method | Million_mutation |