WormBase Tree Display for Variation: WBVar00316696
expand all nodes | collapse all nodes | view schema
WBVar00316696 | Evidence | Paper_evidence | WBPaper00036201 | ||
---|---|---|---|---|---|
Name | Public_name | otn19875 | |||
Other_name | OH9482_90817 | ||||
C29E6.1b.1:c.840+446T>C | |||||
C29E6.1a.1:c.840+446T>C | |||||
C29E6.1c.1:c.840+446T>C | |||||
HGVSg | CHROMOSOME_IV:g.11887421T>C | ||||
Sequence_details | SMap | S_parent | Sequence | C29E6 | |
Flanking_sequences | TTTAAATCAATTAAGTTTTGTTTGTAGATTACAAAAATTGAATCCCGACT | GATTGGACCACACCCAAAACTTTTATAGCCAATCAAAGTCAAAAAGTGAA | |||
Mapping_target | C29E6 | ||||
Type_of_mutation | Substitution | T | C | ||
SeqStatus | Sequenced | ||||
Variation_type | Allele | ||||
Origin | Species | Caenorhabditis elegans | |||
Strain | WBStrain00029572 | ||||
Laboratory | OTN | ||||
Analysis | WGS_Hobert | ||||
Status | Live | ||||
Affects | Gene | WBGene00002827 | |||
Transcript | C29E6.1b.1 | VEP_consequence | intron_variant | ||
VEP_impact | MODIFIER | ||||
HGVSc | C29E6.1b.1:c.840+446T>C | ||||
Intron_number | 5/10 | ||||
C29E6.1a.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | C29E6.1a.1:c.840+446T>C | ||||
Intron_number | 5/11 | ||||
C29E6.1c.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | C29E6.1c.1:c.840+446T>C | ||||
Intron_number | 4/9 | ||||
Genetics | Map | IV | |||
Reference | WBPaper00036201 | ||||
Method | WGS_Hobert |