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WormBase Tree Display for Variation: WBVar01883235

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Name Class

WBVar01883235NamePublic_nameWBVar01883235
Other_namecewivar00597947
T10A3.1b.1:c.995-46A>G
T10A3.1c.1:c.995-46A>G
T10A3.1f.1:c.995-46A>G
T10A3.1e.1:c.995-46A>G
T10A3.1a.1:c.995-46A>G
T10A3.1d.1:c.995-46A>G
HGVSgCHROMOSOME_X:g.7278089T>C
Sequence_detailsSMapS_parentSequenceK03A1
Flanking_sequencesCTATATCAATTTGCGTCTCGTTCGCAATTTAGCGCACAACACTTTTTTGTTTTGTTTTTC
Mapping_targetK03A1
Source_location225CHROMOSOME_X72780447278044From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionTC
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00023072From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00006750
TranscriptT10A3.1c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT10A3.1c.1:c.995-46A>G
Intron_number7/28
T10A3.1d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT10A3.1d.1:c.995-46A>G
Intron_number7/27
T10A3.1e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT10A3.1e.1:c.995-46A>G
Intron_number7/27
T10A3.1b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT10A3.1b.1:c.995-46A>G
Intron_number7/27
T10A3.1a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT10A3.1a.1:c.995-46A>G
Intron_number8/27
T10A3.1f.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT10A3.1f.1:c.995-46A>G
Intron_number7/26
MethodWGS_Flibotte