WormBase Tree Display for Variation: WBVar02126304
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WBVar02126304 | Evidence | Paper_evidence | WBPaper00045317 | |||
---|---|---|---|---|---|---|
Name | Public_name | h9574 | ||||
Other_name | F47G6.1b.1:c.474-424del | |||||
F47G6.1c.1:c.-994-424del | ||||||
F47G6.1a.1:c.708-424del | ||||||
HGVSg | CHROMOSOME_I:g.1486755del | |||||
Sequence_details | SMap | S_parent | Sequence | F47G6 | ||
Flanking_sequences | GGATTTTCAGAGCGGTGTAACTTTTGAAAAACTGTAAAAA | TTTTTTTTAATTCTGCAATAATTGTATCTATAACTTATTC | ||||
Mapping_target | CHROMOSOME_I | |||||
Source_location | 200 | CHROMOSOME_I | 1486756 | 1486756 | ||
Type_of_mutation | Deletion | |||||
SeqStatus | Sequenced | |||||
Variation_type | Allele | |||||
Origin | Species | Caenorhabditis elegans | ||||
Strain | WBStrain00023672 | |||||
Laboratory | KR | |||||
Analysis | WGS_Rose | |||||
Status | Live | |||||
Affects | Gene | WBGene00001115 | ||||
Transcript | F47G6.1c.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | |||||
HGVSc | F47G6.1c.1:c.-994-424del | |||||
Intron_number | 2/8 | |||||
F47G6.1b.1 | VEP_consequence | intron_variant | ||||
VEP_impact | MODIFIER | |||||
HGVSc | F47G6.1b.1:c.474-424del | |||||
Intron_number | 4/8 | |||||
F47G6.1a.1 | VEP_consequence | intron_variant | ||||
VEP_impact | MODIFIER | |||||
HGVSc | F47G6.1a.1:c.708-424del | |||||
Intron_number | 6/11 | |||||
Reference | WBPaper00040589 | |||||
WBPaper00000975 | ||||||
WBPaper00003985 | ||||||
WBPaper00000699 | ||||||
WBPaper00045317 | ||||||
Method | WGS_Rose |