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WormBase Tree Display for Variation: WBVar01784319

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Name Class

WBVar01784319NamePublic_nameWBVar01784319
Other_namecewivar00485336
T24H10.7h.1:c.509+794G>A
T24H10.7b.1:c.647+794G>A
T24H10.7f.1:c.551+794G>A
T24H10.7i.1:c.398+794G>A
T24H10.7g.1:c.275+794G>A
T24H10.7a.1:c.707+794G>A
HGVSgCHROMOSOME_II:g.9124130G>A
Sequence_detailsSMapS_parentSequenceT24H10
Flanking_sequencesTTTGCCTACAAGTTATAAAAATACTTTCAAAAAGTCGAGAGCTCTCAGTTACCACCAAAA
Mapping_targetT24H10
Source_location225CHROMOSOME_II91240689124068From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionGA
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00023192From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00012005
TranscriptT24H10.7g.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT24H10.7g.1:c.275+794G>A
Intron_number2/3
T24H10.7f.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT24H10.7f.1:c.551+794G>A
Intron_number6/8
T24H10.7i.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT24H10.7i.1:c.398+794G>A
Intron_number3/4
T24H10.7h.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT24H10.7h.1:c.509+794G>A
Intron_number4/5
T24H10.7a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT24H10.7a.1:c.707+794G>A
Intron_number7/9
T24H10.7b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT24H10.7b.1:c.647+794G>A
Intron_number7/9
MethodWGS_Flibotte