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WormBase Tree Display for Variation: WBVar00012542

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Name Class

WBVar00012542NamePublic_nameWBVar00012542
Other_namecbv13663
HGVSgchrII:g.4420602C>A
Sequence_detailsSMapS_parentSequencecb25.fpc2441
Flanking_sequencesCACTGAAAACGTCACATTTGATATCTAATGTAACAACTCTTGAATGGCCT
Mapping_targetcb25.fpc2441
Type_of_mutationSubstitutionCA
SeqStatusSequenced
Variation_typeSNP
Predicted_SNP
Natural_variant
OriginSpeciesCaenorhabditis briggsae
StrainWBStrain00042094
LaboratoryCP
PersonWBPerson3706
WBPerson227
WBPerson225
StatusLive
AffectsGeneWBGene00032251
WBGene00032253
TranscriptCBG11064a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScCBG11064a.1:c.1219+618G>T
Intron_number8/31
CBG11064c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScCBG11064c.1:c.1219+618G>T
Intron_number8/45
CBG11064d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScCBG11064d.1:c.1219+618G>T
Intron_number7/31
CBG11064e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScCBG11064e.1:c.1219+618G>T
Intron_number8/27
CBG11064g.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScCBG11064g.1:c.1219+618G>T
Intron_number7/44
CBG11064h.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScCBG11064h.1:c.1219+618G>T
Intron_number7/30
CBG11066.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScCBG11066.1:c.1204-160C>A
Intron_number7/9
MethodSNP