WormBase Tree Display for Variation: WBVar02133152
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WBVar02133152 | Evidence | Paper_evidence | WBPaper00045317 | |||
---|---|---|---|---|---|---|
Name | Public_name | h10920 | ||||
Other_name | T21D12.9c.1:c.*399+27T>A | |||||
T21D12.9a.1:c.2549+27T>A | ||||||
T21D12.9a.2:c.2549+27T>A | ||||||
HGVSg | CHROMOSOME_IV:g.279685T>A | |||||
Sequence_details | SMap | S_parent | Sequence | T21D12 | ||
Flanking_sequences | AGTGCATTTGGACTGTAAGTTTCAAAGATTGTCTAAAATG | TTGTCCTCACTGAAAACCAGTTCATTTTTACAGAATGATT | ||||
Mapping_target | CHROMOSOME_IV | |||||
Source_location | 200 | CHROMOSOME_IV | 279685 | 279685 | ||
Type_of_mutation | Substitution | T | A | |||
SeqStatus | Sequenced | |||||
Variation_type | Allele | |||||
Origin | Species | Caenorhabditis elegans | ||||
Strain | WBStrain00023758 | |||||
Laboratory | KR | |||||
Analysis | WGS_Rose | |||||
Status | Live | |||||
Affects | Gene | WBGene00020649 | ||||
Transcript | T21D12.9a.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | |||||
HGVSc | T21D12.9a.1:c.2549+27T>A | |||||
Intron_number | 13/14 | |||||
T21D12.9c.1 | VEP_consequence | intron_variant | ||||
VEP_impact | MODIFIER | |||||
HGVSc | T21D12.9c.1:c.*399+27T>A | |||||
Intron_number | 14/14 | |||||
T21D12.9a.2 | VEP_consequence | intron_variant | ||||
VEP_impact | MODIFIER | |||||
HGVSc | T21D12.9a.2:c.2549+27T>A | |||||
Intron_number | 14/15 | |||||
Reference | WBPaper00040589 | |||||
WBPaper00000975 | ||||||
WBPaper00003985 | ||||||
WBPaper00000699 | ||||||
WBPaper00045317 | ||||||
Method | WGS_Rose |