WormBase Tree Display for Variation: WBVar01552094
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WBVar01552094 | Name | Public_name | WBVar01552094 | |||||
---|---|---|---|---|---|---|---|---|
Other_name | cewivar00129201 | |||||||
CE43855:p.Asn105Asp | ||||||||
F31B12.1k.1:c.4269+479A>G | ||||||||
F31B12.1i.1:c.4239+479A>G | ||||||||
F31B12.1l.1:c.4098+479A>G | ||||||||
F31B12.1j.1:c.4068+479A>G | ||||||||
F31B12.1g.1:c.4089+479A>G | ||||||||
F31B12.3.1:c.313A>G | ||||||||
F31B12.1h.1:c.4119+479A>G | ||||||||
F31B12.1d.1:c.4260+479A>G | ||||||||
HGVSg | CHROMOSOME_X:g.10820254T>C | |||||||
Sequence_details | SMap | S_parent | Sequence | F31B12 | ||||
Flanking_sequences | AAAAGGGCTTACCAATTGAAGAATGTTCAT | ATAGTTGGAAATAAACTCTTCTAGGTTTCG | ||||||
Mapping_target | F31B12 | |||||||
Source_location | 225 | CHROMOSOME_X | 10820189 | 10820189 | From_analysis | Million_mutation_project_reanalysis | ||
Type_of_mutation | Substitution | T | C | |||||
SeqStatus | Sequenced | |||||||
Variation_type | Natural_variant | |||||||
Origin | Species | Caenorhabditis elegans | ||||||
Strain (11) | ||||||||
Laboratory | VC | |||||||
Analysis | Million_mutation_project_reanalysis | |||||||
Status | Live | |||||||
Affects | Gene | WBGene00001495 | ||||||
WBGene00004036 | ||||||||
Transcript | F31B12.1j.1 | VEP_consequence | intron_variant | |||||
VEP_impact | MODIFIER | |||||||
HGVSc | F31B12.1j.1:c.4068+479A>G | |||||||
Intron_number | 27/63 | |||||||
F31B12.1h.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F31B12.1h.1:c.4119+479A>G | |||||||
Intron_number | 27/63 | |||||||
F31B12.1d.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F31B12.1d.1:c.4260+479A>G | |||||||
Intron_number | 28/64 | |||||||
F31B12.1g.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F31B12.1g.1:c.4089+479A>G | |||||||
Intron_number | 27/63 | |||||||
F31B12.1l.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F31B12.1l.1:c.4098+479A>G | |||||||
Intron_number | 27/63 | |||||||
F31B12.3.1 (12) | ||||||||
F31B12.1i.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F31B12.1i.1:c.4239+479A>G | |||||||
Intron_number | 28/64 | |||||||
F31B12.1k.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F31B12.1k.1:c.4269+479A>G | |||||||
Intron_number | 28/64 | |||||||
Method | WGS_Flibotte |