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WormBase Tree Display for Variation: WBVar01787278

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Name Class

WBVar01787278NamePublic_nameWBVar01787278
Other_namecewivar00489194
H20J18.1c.1:c.400+60A>C
H20J18.1a.3:c.-3+60A>C
H20J18.1a.1:c.-3+60A>C
H20J18.1h.1:c.-3+60A>C
H20J18.1f.1:c.-3+60A>C
H20J18.1f.2:c.-3+60A>C
HGVSgCHROMOSOME_X:g.12513893T>G
Sequence_detailsSMapS_parentSequenceC16D6
Flanking_sequencesCATTTTAGATCAATTAGCAGAAAAGTTTCTGCAATTAAAAATTTTTTTAACGTCAAGCTA
Mapping_targetC16D6
Source_location225CHROMOSOME_X1251382412513824From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionTG
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00022886From_analysisMillion_mutation_project_reanalysis
WBStrain00022887From_analysisMillion_mutation_project_reanalysis
WBStrain00023192From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00004739
TranscriptH20J18.1f.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScH20J18.1f.2:c.-3+60A>C
Intron_number1/13
H20J18.1a.3VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScH20J18.1a.3:c.-3+60A>C
Intron_number2/14
H20J18.1h.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScH20J18.1h.1:c.-3+60A>C
Intron_number1/12
H20J18.1a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScH20J18.1a.1:c.-3+60A>C
Intron_number1/13
H20J18.1f.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScH20J18.1f.1:c.-3+60A>C
Intron_number2/14
H20J18.1c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScH20J18.1c.1:c.400+60A>C
Intron_number2/12
MethodWGS_Flibotte