WormBase Tree Display for Variation: WBVar01552086
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WBVar01552086 | Name | Public_name | WBVar01552086 | |||||
---|---|---|---|---|---|---|---|---|
Other_name | cewivar00129193 | |||||||
F31B12.1d.1:c.5125+21C>T | ||||||||
F31B12.1l.1:c.4963+21C>T | ||||||||
F31B12.1j.1:c.4933+21C>T | ||||||||
F31B12.1g.1:c.4954+21C>T | ||||||||
F31B12.1i.1:c.5104+21C>T | ||||||||
F31B12.1h.1:c.4984+21C>T | ||||||||
F31B12.1k.1:c.5134+21C>T | ||||||||
HGVSg | CHROMOSOME_X:g.10814027G>A | |||||||
Sequence_details | SMap | S_parent | Sequence | F31B12 | ||||
Flanking_sequences | TACAATGCGGAAAACTGTAGGAATGAGACA | AAAACGTAGGAAAAACGTACAGACAGTCGC | ||||||
Mapping_target | F31B12 | |||||||
Source_location | 225 | CHROMOSOME_X | 10813962 | 10813962 | From_analysis | Million_mutation_project_reanalysis | ||
Type_of_mutation | Substitution | G | A | |||||
SeqStatus | Sequenced | |||||||
Variation_type | Natural_variant | |||||||
Origin | Species | Caenorhabditis elegans | ||||||
Strain | WBStrain00004599 | From_analysis | Million_mutation_project_reanalysis | |||||
Laboratory | VC | |||||||
Analysis | Million_mutation_project_reanalysis | |||||||
Status | Live | |||||||
Affects | Gene | WBGene00004036 | ||||||
Transcript | F31B12.1j.1 | VEP_consequence | intron_variant | |||||
VEP_impact | MODIFIER | |||||||
HGVSc | F31B12.1j.1:c.4933+21C>T | |||||||
Intron_number | 34/63 | |||||||
F31B12.1g.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F31B12.1g.1:c.4954+21C>T | |||||||
Intron_number | 34/63 | |||||||
F31B12.1d.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F31B12.1d.1:c.5125+21C>T | |||||||
Intron_number | 35/64 | |||||||
F31B12.1h.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F31B12.1h.1:c.4984+21C>T | |||||||
Intron_number | 34/63 | |||||||
F31B12.1l.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F31B12.1l.1:c.4963+21C>T | |||||||
Intron_number | 34/63 | |||||||
F31B12.1i.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F31B12.1i.1:c.5104+21C>T | |||||||
Intron_number | 35/64 | |||||||
F31B12.1k.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F31B12.1k.1:c.5134+21C>T | |||||||
Intron_number | 35/64 | |||||||
Method | WGS_Flibotte |