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WormBase Tree Display for Variation: WBVar01787284

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Name Class

WBVar01787284NamePublic_nameWBVar01787284
Other_namecewivar00489202
C16D6.4:n.576T>A
H20J18.1f.1:c.-98-4411T>A
H20J18.1c.1:c.305-4411T>A
H20J18.1a.3:c.-98-4411T>A
HGVSgCHROMOSOME_X:g.12518459A>T
Sequence_detailsSMapS_parentSequenceC16D6
Flanking_sequencesCGTAGAACAACGTCAGAAAAAAGGAAAACAAATAATAAATGAAGAATAACAATATGTGAC
Mapping_targetC16D6
Source_location225CHROMOSOME_X1251839012518390From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionAT
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00022883From_analysisMillion_mutation_project_reanalysis
WBStrain00022886From_analysisMillion_mutation_project_reanalysis
WBStrain00022887From_analysisMillion_mutation_project_reanalysis
WBStrain00023192From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00004739
WBGene00219561
TranscriptH20J18.1a.3VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScH20J18.1a.3:c.-98-4411T>A
Intron_number1/14
H20J18.1f.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScH20J18.1f.1:c.-98-4411T>A
Intron_number1/14
C16D6.4VEP_consequencenon_coding_transcript_exon_variant
VEP_impactMODIFIER
HGVScC16D6.4:n.576T>A
cDNA_position576
Exon_number1/1
H20J18.1c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScH20J18.1c.1:c.305-4411T>A
Intron_number1/12
MethodWGS_Flibotte