WormBase Tree Display for Variation: WBVar01497659
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WBVar01497659 | Name | Public_name | gk961922 | |||||
---|---|---|---|---|---|---|---|---|
Other_name | T08A11.1e.1:c.1014+158_1014+211delinsAACTACCAAAAATCGATTTTT | |||||||
T08A11.1b.1:c.1014+158_1014+211delinsAACTACCAAAAATCGATTTTT | ||||||||
T08A11.1c.1:c.1014+158_1014+211delinsAACTACCAAAAATCGATTTTT | ||||||||
T08A11.1h.1:c.1014+158_1014+211delinsAACTACCAAAAATCGATTTTT | ||||||||
T08A11.1f.1:c.1014+158_1014+211delinsAACTACCAAAAATCGATTTTT | ||||||||
T08A11.1d.1:c.1014+158_1014+211delinsAACTACCAAAAATCGATTTTT | ||||||||
T08A11.1g.1:c.1014+158_1014+211delinsAACTACCAAAAATCGATTTTT | ||||||||
T08A11.1a.1:c.1014+158_1014+211delinsAACTACCAAAAATCGATTTTT | ||||||||
HGVSg | CHROMOSOME_III:g.4260671_4260724delinsAAAAATCGATTTTTGGTAGTT | |||||||
Sequence_details | SMap | S_parent | Sequence | T08A11 | ||||
Flanking_sequences | AATGGAAAAATCGATTTTTGGTAGTTTATG | TATTAAATTTTGAGCAATGTTGCGTGAAAA | ||||||
Mapping_target | T08A11 | |||||||
Source_location | 225 | CHROMOSOME_III | 4260644 | 4260697 | From_analysis | Million_mutation_project_reanalysis | ||
Type_of_mutation | Insertion | AAAAATCGATTTTTGGTAGTT | ||||||
Deletion | ||||||||
SeqStatus | Sequenced | |||||||
Variation_type | Allele | |||||||
Origin | Species | Caenorhabditis elegans | ||||||
Strain | WBStrain00037992 | |||||||
Laboratory | VC | |||||||
Analysis | Million_mutation_project_reanalysis | |||||||
Status | Live | |||||||
Affects | Gene | WBGene00011604 | ||||||
Transcript | T08A11.1e.1 | VEP_consequence | intron_variant | |||||
VEP_impact | MODIFIER | |||||||
HGVSc | T08A11.1e.1:c.1014+158_1014+211delinsAACTACCAAAAATCGATTTTT | |||||||
Intron_number | 4/17 | |||||||
T08A11.1g.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | T08A11.1g.1:c.1014+158_1014+211delinsAACTACCAAAAATCGATTTTT | |||||||
Intron_number | 5/18 | |||||||
T08A11.1h.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | T08A11.1h.1:c.1014+158_1014+211delinsAACTACCAAAAATCGATTTTT | |||||||
Intron_number | 5/18 | |||||||
T08A11.1d.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | T08A11.1d.1:c.1014+158_1014+211delinsAACTACCAAAAATCGATTTTT | |||||||
Intron_number | 5/18 | |||||||
T08A11.1f.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | T08A11.1f.1:c.1014+158_1014+211delinsAACTACCAAAAATCGATTTTT | |||||||
Intron_number | 4/17 | |||||||
T08A11.1c.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | T08A11.1c.1:c.1014+158_1014+211delinsAACTACCAAAAATCGATTTTT | |||||||
Intron_number | 4/17 | |||||||
T08A11.1b.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | T08A11.1b.1:c.1014+158_1014+211delinsAACTACCAAAAATCGATTTTT | |||||||
Intron_number | 5/18 | |||||||
T08A11.1a.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | T08A11.1a.1:c.1014+158_1014+211delinsAACTACCAAAAATCGATTTTT | |||||||
Intron_number | 5/18 | |||||||
Reference | WBPaper00042537 | |||||||
Method | Million_mutation |