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WormBase Tree Display for Variation: WBVar01815933

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Name Class

WBVar01815933NamePublic_nameWBVar01815933
Other_namecewivar00527317
T10A3.1c.1:c.69+32C>T
T10A3.1b.1:c.69+32C>T
T10A3.1f.1:c.69+32C>T
T10A3.1d.1:c.69+32C>T
T10A3.1e.1:c.69+32C>T
T10A3.1a.1:c.69+32C>T
HGVSgCHROMOSOME_X:g.7280201G>A
Sequence_detailsSMapS_parentSequenceK03A1
Flanking_sequencesGGGCAAAATGAACGATGGGGGGGGGGGGGGGGGGGAGGGGGTTCGTGCTGGAACAACTCA
Mapping_targetK03A1
Source_location225CHROMOSOME_X72801567280156From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionGA
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00022850From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00006750
TranscriptT10A3.1c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT10A3.1c.1:c.69+32C>T
Intron_number1/28
T10A3.1d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT10A3.1d.1:c.69+32C>T
Intron_number1/27
T10A3.1e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT10A3.1e.1:c.69+32C>T
Intron_number1/27
T10A3.1b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT10A3.1b.1:c.69+32C>T
Intron_number1/27
T10A3.1a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT10A3.1a.1:c.69+32C>T
Intron_number2/27
T10A3.1f.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT10A3.1f.1:c.69+32C>T
Intron_number1/26
MethodWGS_Flibotte