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WormBase Tree Display for Variation: WBVar01527598

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Name Class

WBVar01527598NamePublic_nameWBVar01527598
Other_namecewivar00060833
T06H11.1f.1:c.413-1356A>G
T06H11.1c.1:c.149-1356A>G
T06H11.1e.1:c.67+385A>G
T06H11.1b.1:c.263-1356A>G
T06H11.1d.1:c.293-1356A>G
T06H11.1g.1:c.137-1356A>G
HGVSgCHROMOSOME_X:g.10110687T>C
Sequence_detailsSMapS_parentSequenceT06H11
Flanking_sequencesGCACCTCCGGCGCGGCCCCGACTTCTGGGGTGAAAACTAATTTTTCTGAAACTACCGTAA
Mapping_targetT06H11
Source_location225CHROMOSOME_X1011062810110628From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionTC
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
Strain (36)
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00006792
TranscriptT06H11.1b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT06H11.1b.1:c.263-1356A>G
Intron_number3/12
T06H11.1g.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT06H11.1g.1:c.137-1356A>G
Intron_number2/12
T06H11.1f.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT06H11.1f.1:c.413-1356A>G
Intron_number4/14
T06H11.1e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT06H11.1e.1:c.67+385A>G
Intron_number2/13
T06H11.1d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT06H11.1d.1:c.293-1356A>G
Intron_number1/11
T06H11.1c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT06H11.1c.1:c.149-1356A>G
Intron_number2/13
MethodWGS_Flibotte