WormBase Tree Display for Variation: WBVar00307865
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WBVar00307865 | Evidence | Paper_evidence | WBPaper00036201 | ||
---|---|---|---|---|---|
Name | Public_name | otn11044 | |||
Other_name | OH8421_70358 | ||||
T08A11.1d.1:c.174+48T>C | |||||
T08A11.1c.1:c.174+48T>C | |||||
T08A11.1f.1:c.174+48T>C | |||||
T08A11.1b.1:c.174+48T>C | |||||
T08A11.1a.1:c.174+48T>C | |||||
T08A11.1g.1:c.174+48T>C | |||||
T08A11.1e.1:c.174+48T>C | |||||
T08A11.1h.1:c.174+48T>C | |||||
HGVSg | CHROMOSOME_III:g.4262827A>G | ||||
Sequence_details | SMap | S_parent | Sequence | T08A11 | |
Flanking_sequences | AAACCGGTCTATTGAGGTAATTTGAGTATTTTAACTTTACTTTAATTTTA | TTTTTCAGTATTTTAATGAATAATTCTGTGCCCTATCCATTACGAACCGG | |||
Mapping_target | T08A11 | ||||
Type_of_mutation | Substitution | A | G | ||
SeqStatus | Sequenced | ||||
Variation_type | Allele | ||||
Origin | Species | Caenorhabditis elegans | |||
Strain | WBStrain00029552 | ||||
Laboratory | OTN | ||||
Analysis | WGS_Hobert | ||||
Status | Live | ||||
Affects | Gene | WBGene00011604 | |||
Transcript | T08A11.1e.1 | VEP_consequence | intron_variant | ||
VEP_impact | MODIFIER | ||||
HGVSc | T08A11.1e.1:c.174+48T>C | ||||
Intron_number | 1/17 | ||||
T08A11.1g.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | T08A11.1g.1:c.174+48T>C | ||||
Intron_number | 2/18 | ||||
T08A11.1h.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | T08A11.1h.1:c.174+48T>C | ||||
Intron_number | 2/18 | ||||
T08A11.1d.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | T08A11.1d.1:c.174+48T>C | ||||
Intron_number | 2/18 | ||||
T08A11.1f.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | T08A11.1f.1:c.174+48T>C | ||||
Intron_number | 1/17 | ||||
T08A11.1c.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | T08A11.1c.1:c.174+48T>C | ||||
Intron_number | 1/17 | ||||
T08A11.1b.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | T08A11.1b.1:c.174+48T>C | ||||
Intron_number | 2/18 | ||||
T08A11.1a.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | T08A11.1a.1:c.174+48T>C | ||||
Intron_number | 2/18 | ||||
Genetics | Map | III | |||
Reference | WBPaper00036201 | ||||
Method | WGS_Hobert |