WormBase Tree Display for Variation: WBVar01470482
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WBVar01470482 | Evidence | Paper_evidence | WBPaper00040707 | |||
---|---|---|---|---|---|---|
Name | Public_name | WBVar01470482 | ||||
Other_name | cewivar00060515 | |||||
C23F12.1w.1:c.1215+1069G>A | ||||||
C23F12.1e.1:c.1215+1069G>A | ||||||
C23F12.1a.1:c.1215+1069G>A | ||||||
C23F12.1t.1:c.1215+1069G>A | ||||||
C23F12.1u.1:c.1215+1069G>A | ||||||
C23F12.1r.1:c.1215+1069G>A | ||||||
C23F12.1s.1:c.1215+1069G>A | ||||||
C23F12.1v.1:c.1215+1069G>A | ||||||
HGVSg | CHROMOSOME_X:g.9401741G>A | |||||
Sequence_details | SMap | S_parent | Sequence | C23F12 | ||
Flanking_sequences | TTCATAATTGGTGTTTAAATTTGCCAATTT | CGATTGAAATTTAAAATTTGAATTCAGAAA | ||||
Mapping_target | C23F12 | |||||
Type_of_mutation | Substitution | g | a | |||
SeqStatus | Sequenced | |||||
Variation_type | SNP | |||||
Natural_variant | ||||||
Origin | Species | Caenorhabditis elegans | ||||
Strain (77) | ||||||
Laboratory | QX | |||||
Person | WBPerson1730 | |||||
Analysis | Million_mutation_project_reanalysis | |||||
WGS_Andersen | ||||||
DB_info | Database | dbSNP_rs | rs | 193355784 | ||
dbSNP_ss | ss | 295531703 | ||||
Status | Live | |||||
Affects | Gene | WBGene00016006 | ||||
Transcript | C23F12.1t.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | |||||
HGVSc | C23F12.1t.1:c.1215+1069G>A | |||||
Intron_number | 8/49 | |||||
C23F12.1v.1 | VEP_consequence | intron_variant | ||||
VEP_impact | MODIFIER | |||||
HGVSc | C23F12.1v.1:c.1215+1069G>A | |||||
Intron_number | 8/48 | |||||
C23F12.1u.1 | VEP_consequence | intron_variant | ||||
VEP_impact | MODIFIER | |||||
HGVSc | C23F12.1u.1:c.1215+1069G>A | |||||
Intron_number | 8/45 | |||||
C23F12.1s.1 | VEP_consequence | intron_variant | ||||
VEP_impact | MODIFIER | |||||
HGVSc | C23F12.1s.1:c.1215+1069G>A | |||||
Intron_number | 8/49 | |||||
C23F12.1w.1 | VEP_consequence | intron_variant | ||||
VEP_impact | MODIFIER | |||||
HGVSc | C23F12.1w.1:c.1215+1069G>A | |||||
Intron_number | 8/44 | |||||
C23F12.1r.1 | VEP_consequence | intron_variant | ||||
VEP_impact | MODIFIER | |||||
HGVSc | C23F12.1r.1:c.1215+1069G>A | |||||
Intron_number | 8/46 | |||||
C23F12.1a.1 | VEP_consequence | intron_variant | ||||
VEP_impact | MODIFIER | |||||
HGVSc | C23F12.1a.1:c.1215+1069G>A | |||||
Intron_number | 9/52 | |||||
C23F12.1e.1 | VEP_consequence | intron_variant | ||||
VEP_impact | MODIFIER | |||||
HGVSc | C23F12.1e.1:c.1215+1069G>A | |||||
Intron_number | 8/46 | |||||
Reference | WBPaper00040707 | |||||
Method | WGS_Andersen |