WormBase Tree Display for Variation: WBVar01822367
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WBVar01822367 | Name | Public_name | WBVar01822367 | |||||
---|---|---|---|---|---|---|---|---|
Other_name | cewivar00534132 | |||||||
C33D12.2a.1:c.1632+416A>T | ||||||||
C33D12.2b.4:c.-10+416A>T | ||||||||
C33D12.2b.1:c.-10+416A>T | ||||||||
C33D12.2b.5:c.-10+416A>T | ||||||||
C33D12.2c.1:c.1632+416A>T | ||||||||
C33D12.2b.3:c.-10+416A>T | ||||||||
C33D12.2b.2:c.-10+416A>T | ||||||||
HGVSg | CHROMOSOME_X:g.3041571T>A | |||||||
Sequence_details | SMap | S_parent | Sequence | M02F4 | ||||
Flanking_sequences | CAATGTTTAAATATTAATATTTGTAGCATA | GTAAATCATAAAATTAGGGAAAAATTTTTT | ||||||
Mapping_target | M02F4 | |||||||
Source_location | 225 | CHROMOSOME_X | 3041561 | 3041561 | From_analysis | Million_mutation_project_reanalysis | ||
Type_of_mutation | Substitution | T | A | |||||
SeqStatus | Sequenced | |||||||
Variation_type | Natural_variant | |||||||
Origin | Species | Caenorhabditis elegans | ||||||
Strain | WBStrain00022868 | From_analysis | Million_mutation_project_reanalysis | |||||
WBStrain00022878 | From_analysis | Million_mutation_project_reanalysis | ||||||
Laboratory | VC | |||||||
Analysis | Million_mutation_project_reanalysis | |||||||
Status | Live | |||||||
Affects | Gene | WBGene00016343 | ||||||
Transcript | C33D12.2a.1 | VEP_consequence | intron_variant | |||||
VEP_impact | MODIFIER | |||||||
HGVSc | C33D12.2a.1:c.1632+416A>T | |||||||
Intron_number | 10/15 | |||||||
C33D12.2c.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | C33D12.2c.1:c.1632+416A>T | |||||||
Intron_number | 9/15 | |||||||
C33D12.2b.4 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | C33D12.2b.4:c.-10+416A>T | |||||||
Intron_number | 8/14 | |||||||
C33D12.2b.3 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | C33D12.2b.3:c.-10+416A>T | |||||||
Intron_number | 7/13 | |||||||
C33D12.2b.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | C33D12.2b.1:c.-10+416A>T | |||||||
Intron_number | 9/15 | |||||||
C33D12.2b.5 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | C33D12.2b.5:c.-10+416A>T | |||||||
Intron_number | 2/8 | |||||||
C33D12.2b.2 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | C33D12.2b.2:c.-10+416A>T | |||||||
Intron_number | 7/13 | |||||||
Method | WGS_Flibotte |