WormBase Tree Display for Variation: WBVar01903705
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WBVar01903705 | Name | Public_name | WBVar01903705 | |||||
---|---|---|---|---|---|---|---|---|
Other_name | cewivar00619385 | |||||||
C30D11.1l.1:c.63+2661G>A | ||||||||
C30D11.1n.1:c.63+2661G>A | ||||||||
C30D11.1b.1:c.237+715G>A | ||||||||
C30D11.1i.1:c.10-11741G>A | ||||||||
C30D11.1a.1:c.261+5821G>A | ||||||||
C30D11.1m.1:c.63+2661G>A | ||||||||
C30D11.1k.1:c.63+2661G>A | ||||||||
HGVSg | CHROMOSOME_III:g.4127545G>A | |||||||
Sequence_details | SMap | S_parent | Sequence | C30D11 | ||||
Flanking_sequences | ACGTTACCCGTGGTGATCAATGGGGAGAAG | GTGTTTCACGTGATGTGTAGAAGTGTCTAC | ||||||
Mapping_target | C30D11 | |||||||
Source_location | 225 | CHROMOSOME_III | 4127519 | 4127519 | From_analysis | Million_mutation_project_reanalysis | ||
Type_of_mutation | Substitution | G | A | |||||
SeqStatus | Sequenced | |||||||
Variation_type | Natural_variant | |||||||
Origin | Species | Caenorhabditis elegans | ||||||
Strain | WBStrain00027647 | From_analysis | Million_mutation_project_reanalysis | |||||
Laboratory | VC | |||||||
Analysis | Million_mutation_project_reanalysis | |||||||
Status | Live | |||||||
Affects | Gene | WBGene00006830 | ||||||
Transcript | C30D11.1k.1 | VEP_consequence | intron_variant | |||||
VEP_impact | MODIFIER | |||||||
HGVSc | C30D11.1k.1:c.63+2661G>A | |||||||
Intron_number | 2/16 | |||||||
C30D11.1m.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | C30D11.1m.1:c.63+2661G>A | |||||||
Intron_number | 1/14 | |||||||
C30D11.1n.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | C30D11.1n.1:c.63+2661G>A | |||||||
Intron_number | 1/13 | |||||||
C30D11.1l.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | C30D11.1l.1:c.63+2661G>A | |||||||
Intron_number | 2/15 | |||||||
C30D11.1i.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | C30D11.1i.1:c.10-11741G>A | |||||||
Intron_number | 1/14 | |||||||
C30D11.1b.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | C30D11.1b.1:c.237+715G>A | |||||||
Intron_number | 1/14 | |||||||
C30D11.1a.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | C30D11.1a.1:c.261+5821G>A | |||||||
Intron_number | 1/14 | |||||||
Method | WGS_Flibotte |