WormBase Tree Display for Variation: WBVar00274135
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WBVar00274135 | Evidence | Paper_evidence | WBPaper00005369 | ||
---|---|---|---|---|---|
Name | Public_name | WBVar00274135 | |||
Other_name | uCE6-791 | ||||
C33D12.2b.3:c.-10+821_-10+822insG | |||||
C33D12.2b.5:c.-10+821_-10+822insG | |||||
C33D12.2b.2:c.-10+821_-10+822insG | |||||
C33D12.2b.4:c.-10+821_-10+822insG | |||||
C33D12.2b.1:c.-10+821_-10+822insG | |||||
C33D12.2a.1:c.1632+821_1632+822insG | |||||
C33D12.2c.1:c.1632+821_1632+822insG | |||||
HGVSg | CHROMOSOME_X:g.3041165_3041166insC | ||||
Sequence_details | SMap | S_parent | Sequence | M02F4 | |
Flanking_sequences | ATTTGAATAGAAGCTAGGAAAAACTCGGAAATGAAATGTTTTCAAACTTATTTTTCATTCGTTTAAGCGGATAAAAAATTTATTTGCCACTCACTTTCTG | ATCTAATTTTTCAAAGTTGTTATCAATTTTGAAGTTAAAGTCGGAACATCACCAATTGGAAAATTTTAAAACCTAGTGTTAAATGTCAGTATATCATAATA | |||
Mapping_target | M02F4 | ||||
Type_of_mutation | Insertion | C | |||
SeqStatus | Sequenced | ||||
Variation_type | SNP | ||||
Predicted_SNP | |||||
Natural_variant | |||||
Origin | Species | Caenorhabditis elegans | |||
Strain | WBStrain00004602 | From_analysis | SNP_Swan | ||
Analysis | SNP_Swan | ||||
Status | Live | ||||
Affects | Gene | WBGene00016343 | |||
Transcript | C33D12.2a.1 | VEP_consequence | intron_variant | ||
VEP_impact | MODIFIER | ||||
HGVSc | C33D12.2a.1:c.1632+821_1632+822insG | ||||
Intron_number | 10/15 | ||||
C33D12.2c.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | C33D12.2c.1:c.1632+821_1632+822insG | ||||
Intron_number | 9/15 | ||||
C33D12.2b.4 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | C33D12.2b.4:c.-10+821_-10+822insG | ||||
Intron_number | 8/14 | ||||
C33D12.2b.3 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | C33D12.2b.3:c.-10+821_-10+822insG | ||||
Intron_number | 7/13 | ||||
C33D12.2b.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | C33D12.2b.1:c.-10+821_-10+822insG | ||||
Intron_number | 9/15 | ||||
C33D12.2b.5 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | C33D12.2b.5:c.-10+821_-10+822insG | ||||
Intron_number | 2/8 | ||||
C33D12.2b.2 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | C33D12.2b.2:c.-10+821_-10+822insG | ||||
Intron_number | 7/13 | ||||
Reference | WBPaper00005369 | ||||
Method | SNP_Swan |