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WormBase Tree Display for Variation: WBVar01831283

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Name Class

WBVar01831283NamePublic_nameWBVar01831283
Other_namecewivar00543459
T24H10.7i.1:c.113+583A>G
T24H10.7f.1:c.266+583A>G
T24H10.7h.1:c.224+583A>G
T24H10.7b.1:c.362+583A>G
T24H10.7a.1:c.422+583A>G
HGVSgCHROMOSOME_II:g.9121501A>G
Sequence_detailsSMapS_parentSequenceT24H10
Flanking_sequencesCTCTGCTTACGTCATGCCTTGAAAATTTGTACTCACTAGGTGCGGTAACTTGTAGAAATT
Mapping_targetT24H10
Source_location225CHROMOSOME_II91214399121439From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionAG
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00022887From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00012005
TranscriptT24H10.7f.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT24H10.7f.1:c.266+583A>G
Intron_number4/8
T24H10.7i.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT24H10.7i.1:c.113+583A>G
Intron_number1/4
T24H10.7h.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT24H10.7h.1:c.224+583A>G
Intron_number2/5
T24H10.7a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT24H10.7a.1:c.422+583A>G
Intron_number5/9
T24H10.7b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT24H10.7b.1:c.362+583A>G
Intron_number5/9
MethodWGS_Flibotte