WormBase Tree Display for Variation: WBVar01552063
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WBVar01552063 | Name | Public_name | WBVar01552063 | |||||
---|---|---|---|---|---|---|---|---|
Other_name | cewivar00129170 | |||||||
F31B12.1i.1:c.7864-64G>A | ||||||||
F31B12.1f.1:c.2890-64G>A | ||||||||
F31B12.1h.1:c.7744-64G>A | ||||||||
F31B12.1b.1:c.2836-64G>A | ||||||||
F31B12.1k.1:c.7894-64G>A | ||||||||
F31B12.1d.1:c.7885-64G>A | ||||||||
F31B12.1a.1:c.2836-64G>A | ||||||||
F31B12.1j.1:c.7693-64G>A | ||||||||
F31B12.1g.1:c.7714-64G>A | ||||||||
F31B12.1c.1:c.2836-64G>A | ||||||||
F31B12.1l.1:c.7723-64G>A | ||||||||
F31B12.1e.1:c.2866-64G>A | ||||||||
HGVSg | CHROMOSOME_X:g.10801797C>T | |||||||
Sequence_details | SMap | S_parent | Sequence | F31B12 | ||||
Flanking_sequences | CGCAATGTGCTGTGCAATTTTCATTGTTTG | GGCTTGATGTCTTTGTGTAGGCGGGTGTTA | ||||||
Mapping_target | F31B12 | |||||||
Source_location | 225 | CHROMOSOME_X | 10801732 | 10801732 | From_analysis | Million_mutation_project_reanalysis | ||
Type_of_mutation | Substitution | C | T | |||||
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.7693-64G>A | |||||||
Intron_number | 49/63 | |||||||
F31B12.1f.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F31B12.1f.1:c.2890-64G>A | |||||||
Intron_number | 17/31 | |||||||
F31B12.1h.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F31B12.1h.1:c.7744-64G>A | |||||||
Intron_number | 49/63 | |||||||
F31B12.1c.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F31B12.1c.1:c.2836-64G>A | |||||||
Intron_number | 16/32 | |||||||
F31B12.1d.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F31B12.1d.1:c.7885-64G>A | |||||||
Intron_number | 50/64 | |||||||
F31B12.1g.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F31B12.1g.1:c.7714-64G>A | |||||||
Intron_number | 49/63 | |||||||
F31B12.1b.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F31B12.1b.1:c.2836-64G>A | |||||||
Intron_number | 16/31 | |||||||
F31B12.1a.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F31B12.1a.1:c.2836-64G>A | |||||||
Intron_number | 17/33 | |||||||
F31B12.1e.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F31B12.1e.1:c.2866-64G>A | |||||||
Intron_number | 16/30 | |||||||
F31B12.1l.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F31B12.1l.1:c.7723-64G>A | |||||||
Intron_number | 49/63 | |||||||
F31B12.1i.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F31B12.1i.1:c.7864-64G>A | |||||||
Intron_number | 50/64 | |||||||
F31B12.1k.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F31B12.1k.1:c.7894-64G>A | |||||||
Intron_number | 50/64 | |||||||
Method | WGS_Flibotte |