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WormBase Tree Display for Variation: WBVar00820775

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Name Class

WBVar00820775NamePublic_namegk750513
Other_nameT08A11.1b.1:c.2594-849G>A
T08A11.1e.1:c.2588-849G>A
T08A11.1g.1:c.2588-843G>A
T08A11.1h.1:c.2594-843G>A
T08A11.1d.1:c.2594-843G>A
T08A11.1c.1:c.2588-843G>A
T08A11.1f.1:c.2594-849G>A
T08A11.1a.1:c.2588-849G>A
HGVSgCHROMOSOME_III:g.4254773C>T
Sequence_detailsSMapS_parentSequenceT08A11
Flanking_sequencesAATTTTAAAAAGTTTTCAAAAAAAAATTTAGAAAATTTTTGTAAGGGGTACTTTTGGATTTTTTTTTTCATAAATCGAAAAAAATATTGATACCTAAAAA
Mapping_targetT08A11
Type_of_mutationSubstitutionCT
SeqStatusSequenced
Variation_typeAllele
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00039637
LaboratoryVC
AnalysisMillion_Mutation_Project
StatusLive
AffectsGeneWBGene00011604
TranscriptT08A11.1e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT08A11.1e.1:c.2588-849G>A
Intron_number9/17
T08A11.1g.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT08A11.1g.1:c.2588-843G>A
Intron_number10/18
T08A11.1h.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT08A11.1h.1:c.2594-843G>A
Intron_number10/18
T08A11.1d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT08A11.1d.1:c.2594-843G>A
Intron_number10/18
T08A11.1f.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT08A11.1f.1:c.2594-849G>A
Intron_number9/17
T08A11.1c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT08A11.1c.1:c.2588-843G>A
Intron_number9/17
T08A11.1b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT08A11.1b.1:c.2594-849G>A
Intron_number10/18
T08A11.1a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT08A11.1a.1:c.2588-849G>A
Intron_number10/18
ReferenceWBPaper00042537
MethodMillion_mutation