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WormBase Tree Display for Variation: WBVar01309149

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Name Class

WBVar01309149EvidencePaper_evidenceWBPaper00037807
NamePublic_nameWBVar01309149
Other_namecewivar00508469
T24H10.7g.1:c.275+2808C>T
T24H10.7f.1:c.551+2808C>T
T24H10.7a.1:c.707+2808C>T
T24H10.7i.1:c.398+2808C>T
T24H10.7h.1:c.509+2808C>T
T24H10.7b.1:c.647+2808C>T
HGVSgCHROMOSOME_II:g.9126144C>T
Sequence_detailsSMapS_parentSequenceT24H10
Flanking_sequencesAAAAGAGAAATGACAAATTTCCGGAGAAAAAAGAATTGCACGGCTAATGATCAATTTTCCCAATTCTTGACGAAAATGAAATGACTAGAATACTAACTAC
Mapping_targetT24H10
Type_of_mutationSubstitutioncTPaper_evidenceWBPaper00037807
SeqStatusSequenced
Variation_typeSNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00022850From_analysisMillion_mutation_project_reanalysis
WGS_De_Bono
LaboratoryAX
AnalysisWGS_De_Bono
Million_mutation_project_reanalysis
DB_infoDatabasedbSNP_ssss539166515
StatusLive
AffectsGeneWBGene00012005
TranscriptT24H10.7g.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT24H10.7g.1:c.275+2808C>T
Intron_number2/3
T24H10.7f.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT24H10.7f.1:c.551+2808C>T
Intron_number6/8
T24H10.7i.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT24H10.7i.1:c.398+2808C>T
Intron_number3/4
T24H10.7h.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT24H10.7h.1:c.509+2808C>T
Intron_number4/5
T24H10.7a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT24H10.7a.1:c.707+2808C>T
Intron_number7/9
T24H10.7b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT24H10.7b.1:c.647+2808C>T
Intron_number7/9
ReferenceWBPaper00037807
MethodWGS_De_Bono