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WormBase Tree Display for Variation: WBVar01945653

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Name Class

WBVar01945653NamePublic_nameWBVar01945653
Other_namecewivar00667178
T10A3.1c.1:c.2410+41dup
T10A3.1b.1:c.2449+41dup
T10A3.1d.1:c.2404+41dup
T10A3.1e.1:c.2410+41dup
T10A3.1a.1:c.2449+41dup
T10A3.1f.1:c.2404+41dup
HGVSgCHROMOSOME_X:g.7275582_7275583insA
Sequence_detailsSMapS_parentSequenceT10A3
Flanking_sequencesATTTTAACAAAATGTGAACTATTTTTCATCAAAAAAAAATATCTACACCAAAGTTAACAT
Mapping_targetT10A3
Source_location225CHROMOSOME_X72755377275538From_analysisMillion_mutation_project_reanalysis
Type_of_mutationInsertionA
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00004599From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00006750
TranscriptT10A3.1c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT10A3.1c.1:c.2410+41dup
Intron_number18/28
T10A3.1d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT10A3.1d.1:c.2404+41dup
Intron_number18/27
T10A3.1e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT10A3.1e.1:c.2410+41dup
Intron_number18/27
T10A3.1b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT10A3.1b.1:c.2449+41dup
Intron_number17/27
T10A3.1a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT10A3.1a.1:c.2449+41dup
Intron_number18/27
T10A3.1f.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT10A3.1f.1:c.2404+41dup
Intron_number18/26
MethodWGS_Flibotte