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WormBase Tree Display for Variation: WBVar02116435

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Name Class

WBVar02116435NamePublic_nameWBVar02116435
Other_namecewivar00847205
T07H6.5c.1:c.1450+691_1450+710delinsTAGTTGTTGTTGTTGTTGTTAGTTG
T07H6.5a.1:c.1450+691_1450+710delinsTAGTTGTTGTTGTTGTTGTTAGTTG
T07H6.5b.1:c.1450+691_1450+710delinsTAGTTGTTGTTGTTGTTGTTAGTTG
HGVSgCHROMOSOME_X:g.6288111_6288130delinsCAACTAACAACAACAACAACAACTA
Sequence_detailsSMapS_parentSequenceT07H6
Flanking_sequencesGCTCTTATCATCCCAGTCTGGAACAACTTATATGTCCCCATATCAGTTCTGTGAATTTATTCATCTCAAC
Mapping_targetT07H6
Source_location225CHROMOSOME_X62880756288094From_analysisMillion_mutation_project_reanalysis
Type_of_mutationInsertionCAACTAACAACAACAACAACAACTA
Deletion
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00023072From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00002976
TranscriptT07H6.5b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT07H6.5b.1:c.1450+691_1450+710delinsTAGTTGTTGTTGTTGTTGTTAGTTG
Intron_number10/28
T07H6.5a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT07H6.5a.1:c.1450+691_1450+710delinsTAGTTGTTGTTGTTGTTGTTAGTTG
Intron_number10/13
T07H6.5c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT07H6.5c.1:c.1450+691_1450+710delinsTAGTTGTTGTTGTTGTTGTTAGTTG
Intron_number9/12
MethodWGS_Flibotte