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WormBase Tree Display for Variation: WBVar01775670

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Name Class

WBVar01775670NamePublic_nameWBVar01775670
Other_namecewivar00476299
C01G10.11c.1:c.455-432G>A
C01G10.11d.1:c.308-432G>A
C01G10.11b.1:c.728-432G>A
C01G10.11f.1:c.757+316G>A
C01G10.11a.1:c.728-432G>A
HGVSgCHROMOSOME_V:g.15077920G>A
Sequence_detailsSMapS_parentSequenceC01G10
Flanking_sequencesTGTTATTCGAAATTTTTTAAAATATAAATCACAAATAACCGTGTTATACGGTACCTGGTC
Mapping_targetC01G10
Source_location225CHROMOSOME_V1507790315077903From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionGA
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00023072From_analysisMillion_mutation_project_reanalysis
WBStrain00023191From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00006808
WBGene00305285
TranscriptC01G10.11f.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC01G10.11f.1:c.757+316G>A
Intron_number8/11
C01G10.11d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC01G10.11d.1:c.308-432G>A
Intron_number2/4
C01G10.11b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC01G10.11b.1:c.728-432G>A
Intron_number7/9
C01G10.11a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC01G10.11a.1:c.728-432G>A
Intron_number7/10
C25D7.19
C01G10.11c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC01G10.11c.1:c.455-432G>A
Intron_number4/6
MethodWGS_Flibotte