WormBase Tree Display for Variation: WBVar00914564
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WBVar00914564 | Name | Public_name | gk749908 | ||
---|---|---|---|---|---|
Other_name | C11D2.6o.1:c.80-1915G>A | ||||
C11D2.6p.1:c.80-1915G>A | |||||
C11D2.6n.1:c.80-1915G>A | |||||
C11D2.6l.1:c.26-1915G>A | |||||
C11D2.6m.1:c.80-1915G>A | |||||
C11D2.6i.1:c.26-1915G>A | |||||
C11D2.6k.1:c.26-1915G>A | |||||
C11D2.6j.1:c.26-1915G>A | |||||
HGVSg | CHROMOSOME_IV:g.6173321C>T | ||||
Sequence_details | SMap | S_parent | Sequence | C11D2 | |
Flanking_sequences | ATAACGCGGGGGTAACCGAAATGTCTAGCAAATTGTTTGCTCCGAGAGGT | CTTTTAATTTTGAAATGAGATGAGAAGCAGCAACAAATCTTCTTCTTTAT | |||
Mapping_target | C11D2 | ||||
Type_of_mutation | Substitution | C | T | ||
SeqStatus | Sequenced | ||||
Variation_type | Allele | ||||
Origin | Species | Caenorhabditis elegans | |||
Strain | WBStrain00039636 | ||||
Laboratory | VC | ||||
Analysis | Million_Mutation_Project | ||||
Status | Live | ||||
Affects | Gene | WBGene00006809 | |||
Transcript | C11D2.6o.1 | VEP_consequence | intron_variant | ||
VEP_impact | MODIFIER | ||||
HGVSc | C11D2.6o.1:c.80-1915G>A | ||||
Intron_number | 2/28 | ||||
C11D2.6p.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | C11D2.6p.1:c.80-1915G>A | ||||
Intron_number | 2/28 | ||||
C11D2.6i.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | C11D2.6i.1:c.26-1915G>A | ||||
Intron_number | 1/28 | ||||
C11D2.6l.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | C11D2.6l.1:c.26-1915G>A | ||||
Intron_number | 1/27 | ||||
C11D2.6n.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | C11D2.6n.1:c.80-1915G>A | ||||
Intron_number | 2/27 | ||||
C11D2.6j.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | C11D2.6j.1:c.26-1915G>A | ||||
Intron_number | 1/26 | ||||
C11D2.6m.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | C11D2.6m.1:c.80-1915G>A | ||||
Intron_number | 2/29 | ||||
C11D2.6k.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | C11D2.6k.1:c.26-1915G>A | ||||
Intron_number | 1/27 | ||||
Reference | WBPaper00042537 | ||||
Method | Million_mutation |