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WormBase Tree Display for Variation: WBVar02136565

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Name Class

WBVar02136565EvidencePaper_evidenceWBPaper00045317
NamePublic_nameh4763
Other_nameT07H8.4f.1:c.4312+243G>A
T07H8.4h.1:c.4876+243G>A
T07H8.4d.1:c.4843+243G>A
T07H8.4b.1:c.4867+243G>A
T07H8.4e.1:c.4720+243G>A
T07H8.4a.1:c.4879+243G>A
T07H8.4g.1:c.3670+243G>A
T07H8.4d.2:c.4843+243G>A
HGVSgCHROMOSOME_V:g.6963540G>A
Sequence_detailsSMapS_parentSequenceT07H8
Flanking_sequencesGAAATTTAGGATGACATACTTGGATTTTGTTTAGTTTACTCTTTGAAATGATACATATTTTCCAGAATTGTTCAACAAAA
Mapping_targetCHROMOSOME_V
Source_location200CHROMOSOME_V69635226963522
Type_of_mutationSubstitutionGA
SeqStatusSequenced
Variation_typeAllele
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00023661
LaboratoryKR
AnalysisWGS_Rose
StatusLive
AffectsGeneWBGene00003165
TranscriptT07H8.4e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT07H8.4e.1:c.4720+243G>A
Intron_number22/27
T07H8.4b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT07H8.4b.1:c.4867+243G>A
Intron_number24/25
T07H8.4a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT07H8.4a.1:c.4879+243G>A
Intron_number25/31
T07H8.4h.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT07H8.4h.1:c.4876+243G>A
Intron_number24/29
T07H8.4d.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT07H8.4d.2:c.4843+243G>A
Intron_number25/30
T07H8.4f.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT07H8.4f.1:c.4312+243G>A
Intron_number24/29
T07H8.4g.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT07H8.4g.1:c.3670+243G>A
Intron_number16/21
T07H8.4d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT07H8.4d.1:c.4843+243G>A
Intron_number25/31
ReferenceWBPaper00040589
WBPaper00000975
WBPaper00003985
WBPaper00000699
WBPaper00045317
MethodWGS_Rose