WormBase Tree Display for Variation: WBVar02133167
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WBVar02133167 | Evidence | Paper_evidence | WBPaper00045317 | |||
---|---|---|---|---|---|---|
Name | Public_name | h16158 | ||||
Other_name | F18F11.3e.1:c.256-1366T>A | |||||
F18F11.3c.1:c.256-1366T>A | ||||||
F18F11.3b.1:c.256-1366T>A | ||||||
F18F11.3f.1:c.256-1366T>A | ||||||
F18F11.3g.1:c.256-1366T>A | ||||||
F18F11.3a.1:c.256-1366T>A | ||||||
F18F11.3d.1:c.256-1366T>A | ||||||
F18F11.3h.1:c.256-1366T>A | ||||||
HGVSg | CHROMOSOME_IV:g.343807T>A | |||||
Sequence_details | SMap | S_parent | Sequence | F18F11 | ||
Flanking_sequences | CTGCTACGGAGTGTCATCAGTGGGTAGACACTTATTATAG | AGAAAAAACAATACCTGAAACAAATACTCCAAAAAAAATT | ||||
Mapping_target | CHROMOSOME_IV | |||||
Source_location | 200 | CHROMOSOME_IV | 343807 | 343807 | ||
Type_of_mutation | Substitution | T | A | |||
SeqStatus | Sequenced | |||||
Variation_type | Allele | |||||
Origin | Species | Caenorhabditis elegans | ||||
Strain | WBStrain00023750 | |||||
Laboratory | KR | |||||
Analysis | WGS_Rose | |||||
Status | Live | |||||
Affects | Gene | WBGene00017576 | ||||
Transcript | F18F11.3e.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | |||||
HGVSc | F18F11.3e.1:c.256-1366T>A | |||||
Intron_number | 3/25 | |||||
F18F11.3g.1 | VEP_consequence | intron_variant | ||||
VEP_impact | MODIFIER | |||||
HGVSc | F18F11.3g.1:c.256-1366T>A | |||||
Intron_number | 3/25 | |||||
F18F11.3f.1 | VEP_consequence | intron_variant | ||||
VEP_impact | MODIFIER | |||||
HGVSc | F18F11.3f.1:c.256-1366T>A | |||||
Intron_number | 3/24 | |||||
F18F11.3h.1 | VEP_consequence | intron_variant | ||||
VEP_impact | MODIFIER | |||||
HGVSc | F18F11.3h.1:c.256-1366T>A | |||||
Intron_number | 3/26 | |||||
F18F11.3d.1 | VEP_consequence | intron_variant | ||||
VEP_impact | MODIFIER | |||||
HGVSc | F18F11.3d.1:c.256-1366T>A | |||||
Intron_number | 3/25 | |||||
F18F11.3a.1 | VEP_consequence | intron_variant | ||||
VEP_impact | MODIFIER | |||||
HGVSc | F18F11.3a.1:c.256-1366T>A | |||||
Intron_number | 3/25 | |||||
F18F11.3b.1 | VEP_consequence | intron_variant | ||||
VEP_impact | MODIFIER | |||||
HGVSc | F18F11.3b.1:c.256-1366T>A | |||||
Intron_number | 3/23 | |||||
F18F11.3c.1 | VEP_consequence | intron_variant | ||||
VEP_impact | MODIFIER | |||||
HGVSc | F18F11.3c.1:c.256-1366T>A | |||||
Intron_number | 3/24 | |||||
Reference | WBPaper00040589 | |||||
WBPaper00000975 | ||||||
WBPaper00003985 | ||||||
WBPaper00000699 | ||||||
WBPaper00045317 | ||||||
Method | WGS_Rose |