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WormBase Tree Display for Variation: WBVar01568596

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Name Class

WBVar01568596NamePublic_nameWBVar01568596
Other_namecewivar00154374
W02C12.3d.2:c.186+2371G>T
W02C12.3d.1:c.186+2371G>T
W02C12.3j.1:c.213+2371G>T
W02C12.3i.1:c.213+2371G>T
W02C12.3b.1:c.366+2371G>T
W02C12.3c.1:c.366+2371G>T
W02C12.3e.1:c.186+2371G>T
HGVSgCHROMOSOME_IV:g.4024507C>A
Sequence_detailsSMapS_parentSequenceW02C12
Flanking_sequencesCTTTCGTTCTTTTCTATTTTGTTACTTCGTTTTTTTCTTTAATTGTTCAGAAGTACATTT
Mapping_targetW02C12
Source_location225CHROMOSOME_IV40245014024501From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionCA
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00004600From_analysisMillion_mutation_project_reanalysis
WBStrain00022868From_analysisMillion_mutation_project_reanalysis
WBStrain00023018From_analysisMillion_mutation_project_reanalysis
WBStrain00024204From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00020930
TranscriptW02C12.3e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScW02C12.3e.1:c.186+2371G>T
Intron_number1/9
W02C12.3d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScW02C12.3d.1:c.186+2371G>T
Intron_number1/10
W02C12.3j.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScW02C12.3j.1:c.213+2371G>T
Intron_number2/9
W02C12.3b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScW02C12.3b.1:c.366+2371G>T
Intron_number3/11
W02C12.3c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScW02C12.3c.1:c.366+2371G>T
Intron_number3/12
W02C12.3i.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScW02C12.3i.1:c.213+2371G>T
Intron_number2/10
W02C12.3d.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScW02C12.3d.2:c.186+2371G>T
Intron_number2/11
MethodWGS_Flibotte