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WormBase Tree Display for Variation: WBVar02123242

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Name Class

WBVar02123242NamePublic_nameWBVar02123242
Other_namecewivar00854165
HGVSgCHROMOSOME_IV:g.2796003_2806002del
Sequence_detailsSMapS_parentSequenceY54G2A
Flanking_sequencesAAATTTCGGGAAATCTAATTTTTAAAAGTTTTTTCAGCTACTGTGCAGACTCAAAGCTTT
Mapping_targetY54G2A
Source_location225CHROMOSOME_IV27960012806000From_analysisMillion_mutation_project_reanalysis
Type_of_mutationDeletion
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00022850From_analysisMillion_mutation_project_reanalysis
WBStrain00027662From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00021868
WBGene00201830
WBGene00044488
WBGene00021894
WBGene00023179
WBGene00045397
WBGene00021875
WBGene00044487
WBGene00199591
WBGene00023178
WBGene00023180
WBGene00023182
TranscriptY54G2A.10b.2VEP_consequencetranscript_ablation
VEP_impactHIGH
Intron_number2/3
Exon_number1-4/4
Y54G2A.32.2VEP_consequencetranscript_ablation
VEP_impactHIGH
Intron_number1-6/7
Exon_number1-8/8
Y54G2A.2d.1VEP_consequencesplice_acceptor_variant,coding_sequence_variant,3_prime_UTR_variant,intron_variant
VEP_impactHIGH
Intron_number1/1
Exon_number2/2
Y54G2A.65VEP_consequencetranscript_ablation
VEP_impactHIGH
Exon_number1/1
Y54G2A.t1VEP_consequencetranscript_ablation
VEP_impactHIGH
Exon_number1/1
Y54G2A.10a.1VEP_consequencetranscript_ablation
VEP_impactHIGH
Intron_number2-4/5
Exon_number1-6/6
Y54G2A.t5VEP_consequencetranscript_ablation
VEP_impactHIGH
Exon_number1/1
Y54G2A.10b.1VEP_consequencetranscript_ablation
VEP_impactHIGH
Intron_number1-3/4
Exon_number1-5/5
Y54G2A.32.1VEP_consequencetranscript_ablation
VEP_impactHIGH
Intron_number1-4/5
Exon_number1-6/6
Y54G2A.2b.1VEP_consequencesplice_acceptor_variant,coding_sequence_variant,3_prime_UTR_variant,intron_variant
VEP_impactHIGH
Intron_number10/11
Exon_number11-12/12
Y54G2A.2c.1VEP_consequencesplice_acceptor_variant,coding_sequence_variant,3_prime_UTR_variant,intron_variant
VEP_impactHIGH
Intron_number4/4
Exon_number5/5
Y54G2A.t2VEP_consequencetranscript_ablation
VEP_impactHIGH
Exon_number1/1
Y54G2A.44.1VEP_consequencetranscript_ablation
VEP_impactHIGH
Intron_number2-6/7
Exon_number1-8/8
Y54G2A.2a.1VEP_consequencesplice_acceptor_variant,coding_sequence_variant,3_prime_UTR_variant,intron_variant
VEP_impactHIGH
Intron_number10/11
Exon_number11-12/12
Y54G2A.52.1VEP_consequencetranscript_ablation
VEP_impactHIGH
Intron_number2-4/5
Exon_number1-6/6
Y54G2A.t3VEP_consequencetranscript_ablation
VEP_impactHIGH
Exon_number1/1
Y54G2A.70VEP_consequencetranscript_ablation
VEP_impactHIGH
Exon_number1/1
Y54G2A.45a.1VEP_consequencesplice_donor_variant,coding_sequence_variant,5_prime_UTR_variant,intron_variant
VEP_impactHIGH
Intron_number2/9
Exon_number1-2/10
RemarkThe 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
MethodWGS_Flibotte