WormBase Tree Display for Variation: WBVar01620964
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WBVar01620964 | Name | Public_name | WBVar01620964 | |||||
---|---|---|---|---|---|---|---|---|
Other_name | cewivar00300685 | |||||||
C34E11.2g.1:c.1514-926T>C | ||||||||
C34E11.2e.1:c.1796-453T>C | ||||||||
C34E11.2b.1:c.1529-453T>C | ||||||||
C34E11.2f.1:c.1514-453T>C | ||||||||
C34E11.2c.1:c.1697-453T>C | ||||||||
C34E11.2a.1:c.1796-453T>C | ||||||||
C34E11.2d.1:c.1514-453T>C | ||||||||
HGVSg | CHROMOSOME_X:g.11808369A>G | |||||||
Sequence_details | SMap | S_parent | Sequence | C34E11 | ||||
Flanking_sequences | TATTAGAACGTTGTACAATGGAGCACGCTT | CAGACACTATTTTTCTAATTATCAGTTTTC | ||||||
Mapping_target | C34E11 | |||||||
Source_location | 225 | CHROMOSOME_X | 11808301 | 11808301 | From_analysis | Million_mutation_project_reanalysis | ||
Type_of_mutation | Substitution | A | G | |||||
SeqStatus | Sequenced | |||||||
Variation_type | Natural_variant | |||||||
Origin | Species | Caenorhabditis elegans | ||||||
Strain (16) | ||||||||
Laboratory | VC | |||||||
Analysis | Million_mutation_project_reanalysis | |||||||
Status | Live | |||||||
Affects | Gene | WBGene00007935 | ||||||
Transcript | C34E11.2c.1 | VEP_consequence | intron_variant | |||||
VEP_impact | MODIFIER | |||||||
HGVSc | C34E11.2c.1:c.1697-453T>C | |||||||
Intron_number | 10/13 | |||||||
C34E11.2g.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | C34E11.2g.1:c.1514-926T>C | |||||||
Intron_number | 10/12 | |||||||
C34E11.2b.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | C34E11.2b.1:c.1529-453T>C | |||||||
Intron_number | 9/12 | |||||||
C34E11.2a.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | C34E11.2a.1:c.1796-453T>C | |||||||
Intron_number | 11/15 | |||||||
C34E11.2f.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | C34E11.2f.1:c.1514-453T>C | |||||||
Intron_number | 11/15 | |||||||
C34E11.2e.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | C34E11.2e.1:c.1796-453T>C | |||||||
Intron_number | 11/15 | |||||||
C34E11.2d.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | C34E11.2d.1:c.1514-453T>C | |||||||
Intron_number | 10/14 | |||||||
Method | WGS_Flibotte |