WormBase Tree Display for Variation: WBVar00317090
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WBVar00317090 | Evidence | Paper_evidence | WBPaper00036201 | ||
---|---|---|---|---|---|
Name | Public_name | otn20269 | |||
Other_name | OH9482_145779 | ||||
T07H6.5b.1:c.1451-802G>T | |||||
T07H6.5c.1:c.1451-802G>T | |||||
T07H6.5a.1:c.1451-802G>T | |||||
HGVSg | CHROMOSOME_X:g.6287847C>A | ||||
Sequence_details | SMap | S_parent | Sequence | T07H6 | |
Flanking_sequences | ATTTTGGTCAGTGCACTACAAGTGGTCAGTGCAAATGCAAGTGATCAGTG | ACTACAACTGGTCAGTGCAAATGCAGGTGGTCAGTGCAATCGCAAGTGGT | |||
Mapping_target | T07H6 | ||||
Type_of_mutation | Substitution | C | A | ||
SeqStatus | Sequenced | ||||
Variation_type | Allele | ||||
Origin | Species | Caenorhabditis elegans | |||
Strain | WBStrain00029572 | ||||
Laboratory | OTN | ||||
Analysis | WGS_Hobert | ||||
Status | Live | ||||
Affects | Gene | WBGene00002976 | |||
Transcript | T07H6.5b.1 | VEP_consequence | intron_variant | ||
VEP_impact | MODIFIER | ||||
HGVSc | T07H6.5b.1:c.1451-802G>T | ||||
Intron_number | 10/28 | ||||
T07H6.5a.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | T07H6.5a.1:c.1451-802G>T | ||||
Intron_number | 10/13 | ||||
T07H6.5c.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | T07H6.5c.1:c.1451-802G>T | ||||
Intron_number | 9/12 | ||||
Genetics | Map | X | |||
Reference | WBPaper00036201 | ||||
Method | WGS_Hobert |