WormBase Tree Display for Variation: WBVar02123242
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WBVar02123242 | Name | Public_name | WBVar02123242 | |||||
---|---|---|---|---|---|---|---|---|
Other_name | cewivar00854165 | |||||||
HGVSg | CHROMOSOME_IV:g.2796003_2806002del | |||||||
Sequence_details | SMap | S_parent | Sequence | Y54G2A | ||||
Flanking_sequences | AAATTTCGGGAAATCTAATTTTTAAAAGTT | TTTTCAGCTACTGTGCAGACTCAAAGCTTT | ||||||
Mapping_target | Y54G2A | |||||||
Source_location | 225 | CHROMOSOME_IV | 2796001 | 2806000 | From_analysis | Million_mutation_project_reanalysis | ||
Type_of_mutation | Deletion | |||||||
SeqStatus | Sequenced | |||||||
Variation_type | Natural_variant | |||||||
Origin | Species | Caenorhabditis elegans | ||||||
Strain | WBStrain00022850 | From_analysis | Million_mutation_project_reanalysis | |||||
WBStrain00027662 | From_analysis | Million_mutation_project_reanalysis | ||||||
Laboratory | VC | |||||||
Analysis | Million_mutation_project_reanalysis | |||||||
Status | Live | |||||||
Affects | Gene | WBGene00021868 | ||||||
WBGene00201830 | ||||||||
WBGene00044488 | ||||||||
WBGene00021894 | ||||||||
WBGene00023179 | ||||||||
WBGene00045397 | ||||||||
WBGene00021875 | ||||||||
WBGene00044487 | ||||||||
WBGene00199591 | ||||||||
WBGene00023178 | ||||||||
WBGene00023180 | ||||||||
WBGene00023182 | ||||||||
Transcript | Y54G2A.10b.2 | VEP_consequence | transcript_ablation | |||||
VEP_impact | HIGH | |||||||
Intron_number | 2/3 | |||||||
Exon_number | 1-4/4 | |||||||
Y54G2A.32.2 | VEP_consequence | transcript_ablation | ||||||
VEP_impact | HIGH | |||||||
Intron_number | 1-6/7 | |||||||
Exon_number | 1-8/8 | |||||||
Y54G2A.2d.1 | VEP_consequence | splice_acceptor_variant,coding_sequence_variant,3_prime_UTR_variant,intron_variant | ||||||
VEP_impact | HIGH | |||||||
Intron_number | 1/1 | |||||||
Exon_number | 2/2 | |||||||
Y54G2A.65 | VEP_consequence | transcript_ablation | ||||||
VEP_impact | HIGH | |||||||
Exon_number | 1/1 | |||||||
Y54G2A.t1 | VEP_consequence | transcript_ablation | ||||||
VEP_impact | HIGH | |||||||
Exon_number | 1/1 | |||||||
Y54G2A.10a.1 | VEP_consequence | transcript_ablation | ||||||
VEP_impact | HIGH | |||||||
Intron_number | 2-4/5 | |||||||
Exon_number | 1-6/6 | |||||||
Y54G2A.t5 | VEP_consequence | transcript_ablation | ||||||
VEP_impact | HIGH | |||||||
Exon_number | 1/1 | |||||||
Y54G2A.10b.1 | VEP_consequence | transcript_ablation | ||||||
VEP_impact | HIGH | |||||||
Intron_number | 1-3/4 | |||||||
Exon_number | 1-5/5 | |||||||
Y54G2A.32.1 | VEP_consequence | transcript_ablation | ||||||
VEP_impact | HIGH | |||||||
Intron_number | 1-4/5 | |||||||
Exon_number | 1-6/6 | |||||||
Y54G2A.2b.1 | VEP_consequence | splice_acceptor_variant,coding_sequence_variant,3_prime_UTR_variant,intron_variant | ||||||
VEP_impact | HIGH | |||||||
Intron_number | 10/11 | |||||||
Exon_number | 11-12/12 | |||||||
Y54G2A.2c.1 | VEP_consequence | splice_acceptor_variant,coding_sequence_variant,3_prime_UTR_variant,intron_variant | ||||||
VEP_impact | HIGH | |||||||
Intron_number | 4/4 | |||||||
Exon_number | 5/5 | |||||||
Y54G2A.t2 | VEP_consequence | transcript_ablation | ||||||
VEP_impact | HIGH | |||||||
Exon_number | 1/1 | |||||||
Y54G2A.44.1 | VEP_consequence | transcript_ablation | ||||||
VEP_impact | HIGH | |||||||
Intron_number | 2-6/7 | |||||||
Exon_number | 1-8/8 | |||||||
Y54G2A.2a.1 | VEP_consequence | splice_acceptor_variant,coding_sequence_variant,3_prime_UTR_variant,intron_variant | ||||||
VEP_impact | HIGH | |||||||
Intron_number | 10/11 | |||||||
Exon_number | 11-12/12 | |||||||
Y54G2A.52.1 | VEP_consequence | transcript_ablation | ||||||
VEP_impact | HIGH | |||||||
Intron_number | 2-4/5 | |||||||
Exon_number | 1-6/6 | |||||||
Y54G2A.t3 | VEP_consequence | transcript_ablation | ||||||
VEP_impact | HIGH | |||||||
Exon_number | 1/1 | |||||||
Y54G2A.70 | VEP_consequence | transcript_ablation | ||||||
VEP_impact | HIGH | |||||||
Exon_number | 1/1 | |||||||
Y54G2A.45a.1 | VEP_consequence | splice_donor_variant,coding_sequence_variant,5_prime_UTR_variant,intron_variant | ||||||
VEP_impact | HIGH | |||||||
Intron_number | 2/9 | |||||||
Exon_number | 1-2/10 | |||||||
Remark | The boundaries of this variant have been identified only approximately | |||||||
This allele is a copy number variation determined from whole-genome sequence data, and should be assumed to be non-homozygous | ||||||||
Method | WGS_Flibotte |