WormBase Tree Display for Variation: WBVar02139661
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WBVar02139661 | Evidence | Paper_evidence | WBPaper00045317 | |||
---|---|---|---|---|---|---|
Name | Public_name | h10697 | ||||
Other_name | C18A11.7a.1:c.1161+6C>T | |||||
C18A11.7b.1:c.213+6C>T | ||||||
HGVSg | CHROMOSOME_X:g.8052361G>A | |||||
Sequence_details | SMap | S_parent | Sequence | C18A11 | ||
Flanking_sequences | TCGTTTCGGAACTAAGACAAAGAGAGATGCAAAAAATGGG | CTTACCTTGATTGTGAGGATGGCTGAGTAGCTGTCGCTTC | ||||
Mapping_target | CHROMOSOME_X | |||||
Source_location | 200 | CHROMOSOME_X | 8052304 | 8052304 | ||
Type_of_mutation | Substitution | G | A | |||
SeqStatus | Sequenced | |||||
Variation_type | Allele | |||||
Origin | Species | Caenorhabditis elegans | ||||
Strain | WBStrain00023760 | |||||
Laboratory | KR | |||||
Analysis | WGS_Rose | |||||
Status | Live | |||||
Affects | Gene | WBGene00001000 | ||||
Transcript | C18A11.7a.1 | VEP_consequence | splice_region_variant,intron_variant | |||
VEP_impact | LOW | |||||
HGVSc | C18A11.7a.1:c.1161+6C>T | |||||
Intron_number | 9/13 | |||||
C18A11.7b.1 | VEP_consequence | splice_region_variant,intron_variant | ||||
VEP_impact | LOW | |||||
HGVSc | C18A11.7b.1:c.213+6C>T | |||||
Intron_number | 3/7 | |||||
Reference | WBPaper00040589 | |||||
WBPaper00000975 | ||||||
WBPaper00003985 | ||||||
WBPaper00000699 | ||||||
WBPaper00045317 | ||||||
Method | WGS_Rose |