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WormBase Tree Display for Variation: WBVar01622626

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Name Class

WBVar01622626NamePublic_nameWBVar01622626
Other_namecewivar00302448
Y39G10AR.2b.1:c.1061+143G>T
Y39G10AR.2a.1:c.1061+143G>T
Y39G10AR.2c.1:c.98+143G>T
Y39G10AR.2d.1:c.98+143G>T
HGVSgCHROMOSOME_I:g.2406741G>T
Sequence_detailsSMapS_parentSequenceY39G10AR
Flanking_sequencesGCCGAATAATTATTAGAGCGCGCTTGCTGCCTTCGCATTTCTGCATCCGCGGAATTTTGA
Mapping_targetY39G10AR
Source_location225CHROMOSOME_I24067432406743From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionGT
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00006625From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00021460
TranscriptY39G10AR.2a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY39G10AR.2a.1:c.1061+143G>T
Intron_number6/8
Y39G10AR.2b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY39G10AR.2b.1:c.1061+143G>T
Intron_number6/8
Y39G10AR.2d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY39G10AR.2d.1:c.98+143G>T
Intron_number1/2
Y39G10AR.2c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY39G10AR.2c.1:c.98+143G>T
Intron_number1/2
MethodWGS_Flibotte